#chromogenic colour

[brianrope]

Sanctuary

Photography Exhibition Review SANCTUARY | 25 Artists Sutton Village Gallery | 1 – 23 June 2024 The goal of this exhibition is to present a wide range of viewpoints about sanctuary. Australian and international artists honour the history of photography and the skill that goes into making images using traditional printing methods. The labour-intensive methods have produced handmade prints with…

[abwwia]

Isa Genzken, Spielautomat, 1999–2000, slot machine, paper, chromogenic colour prints, tape, plastic foil, 160 × 65 × 50 cm. Courtesy: Galerie Buchholz and © VG Bild-Kunst, Bonn

[thinkingimages]

Simryn Gill | Dalam, 2001

Type C (chromogenic colour print) photograph, set of 260

Dalam (Malay for ‘deep’, or ‘within’) is a suite of 260 photographic images, the result of Malaysian artist Simryn Gill’s sojourn across her home country over an eight-week period. She went up to the homes of complete strangers and asked to photograph their living spaces. Dalam is an expansive yet uncannily intimate survey of Malaysia at the turn of the century, a mélange of disparate ethnicities, religions, ideologies and allegiances. The title itself alludes to the depiction of interior spaces as signifiers of the individual lives that inhabit and activate them, but, even more importantly, it suggests an exploration of the social fabric of contemporary Malaysia. As the artist observes: “In conceiving the work I had wondered what the 'inside' of a place might look like. Do lots of people held together by geography add up to the idea of a nation or single unified group?” Dalam questions what historian Benedict Anderson famously dubbed “the imagined community”, or the various divergent structures that shape the modern nation-state.

Simryn Gill (b. 1959, Singapore) grew up in Malaysia and moved to Australia in 1996. Her work often deals with the historical legacies of migration, and with the realities of life in the tropics. She has exhibited extensively worldwide, with solo exhibitions at Tate Modern, London and the Smithsonian Institution, amongst others. She represented Australia in the Venice Biennale of 2013. 

[earthpiecevii]

Scott Rucker, Untitled (Buffalo, 1978), 1978, chromogenic colour print

[dentalservices]

What Foods and Drinks Cause Teeth Stains?

Teeth stains are a common concern for many people. Despite maintaining good oral hygiene, certain foods and drinks can diminish the natural whiteness of your teeth. Understanding the primary culprits behind these stains can help you make informed choices to preserve a bright smile. In this article, we’ll explore the foods and drinks most likely to cause teeth stains, along with tips on prevention and management.

Why Do Teeth Get Stained?

Before delving into specific items, it’s crucial to grasp why teeth become stained. The outer layer of your teeth, enamel, can be discoloured due to various factors:

Chromogens: These compounds give foods and drinks their colour and can attach to enamel, causing stains.

Tannins: Found in beverages like tea, they enhance chromogens’ ability to adhere to teeth.

Acidity: Foods and drinks with high acidity can erode enamel, making it more susceptible to staining.

Foods That Stain Your Teeth

1. Berries

Berries such as blueberries, blackberries, and cherries, despite their nutritional benefits, contain dark pigments and chromogens that can lead to noticeable discolouration.

Tip: Rinse your mouth with water after consuming berries to mitigate staining.

2. Tomato-Based Sauces

Sauces like pasta sauce and ketchup, due to their acidic nature and deep red colour, are notorious for staining teeth.

Tip: Pair these sauces with leafy greens to counteract their staining effects.

Drinks That Stain Your Teeth

1. Coffee and Tea

Coffee and tea, especially black tea, contain tannins and chromogens that adhere to enamel, causing stains over time.

Tip: Adding milk to your coffee or tea can reduce their staining potential.

2. Red Wine

The rich colour and tannins in red wine contribute significantly to teeth stains, even after just one glass.

Tip: Drink water alongside red wine to minimise staining.

Preventing and Managing Teeth Stains

1. Maintain Good Oral Hygiene

Brushing your teeth twice daily and flossing regularly are essential habits to preserve a bright smile and reduce staining.

2. Visit Your Dentist Regularly

Regular dental check-ups and professional cleanings help remove surface stains and prevent more stubborn discolouration.

Consider Teeth Whitening

For existing stains, teeth whitening near me services offer effective solutions to restore teeth to their natural whiteness.

Knowing which foods and drinks contribute to teeth stains empowers you to make informed dietary choices. By implementing these tips and maintaining good oral hygiene practices, you can effectively prevent and manage teeth stains. If you’re seeking solutions for existing stains, explore teeth whitening near me options to achieve a brighter smile.

[kaylawilliams-photography-631]

Thomas Ruff

I came across Thomas Ruff's work in a book I was looking at in the AUT library. The project below was photos of a number of friends and aqquaitances of the photographer on plain coloured backdrops (the colour chosen by the person subject). The story and rationale behind the photographs was what I found the most fascinating. I also love the idea that he revisited the same people 10-15 years after the initial series of photos was taken but using a plain backdrop the second time - to distinguish the two series.

What I appreciate about Thoma's work here is the simplicity of taken very simply a series of headshots. But that even in how simple they are they show this interesting sense of character about the individual via the position of their head, slight expression and choice of background colour.

In terms of how I could explore this as a series of portraits - this would be great fun to do with friends I have made at university and unitilise the learning I have from the studio to capture a series of very simple portraits.

Chromogenic color prints executed in two sizes

Print size: 24 x 18 cm / Edition: unlimited / Signed and dated in pencil on the reverse

Diasec face, wooden frame / Framed size: 210 x 165 cm, as well as a few special sizes (Edition (1986–91): 2, 3, or 4 + AP / Edition (since 1998): 4 + 2 AP) Signed, dated, and numbered in pencil on the reverse

The idea was to photograph each person as if she or he were a plaster bust, because, according to Ruff, a photograph only reproduces the surface of things anyway. The portraits were taken with the sitters wearing their everyday clothes and with a calm and serious look on their faces. Any form of emotional involvement such as smiles, grins, or flirting with the camera was eschewed. Ruff intuitively chose as models for the portraits persons he actually knew: friends and acquaintances of his own age whom he had met at the academy or in Düsseldorf’s nightlife (on “Ratinger Strasse”).

The objective of the series was to create roughly 100 portraits sized 24 x 18 cm that could be hung in a row like an ancestral portrait gallery. In order to ensure that the series did not become too monotonous owing to the identical background, Ruff initially used a principle culled from the press and which he had discovered while researching the project.

Since he did not want to decide which color went with which person, the persons portrayed were asked to choose their own background, in front of which he then photographed them from different angles (frontally, in profile, and in semi-profile).

In 1991, he was forced to discontinue the series as the photographic paper he had been using for his prints ceased to be available. In 1998, he returned to the theme of portraits and began a new test series to find a combination of film, developing process, and photographic paper that suited his portraits. In this way, he sought to establish whether it was legitimate to imitate one’s own work and whether the now 20 to 35-year-olds looked different than they had when he had portrayed them 10-15 years earlier.

[oaresearchpaper]

Candida Species Identification in Resource-Limited Clinical Settings

Abstract

Candidiasis is worldwide in distribution, and is one of the common fungal diseases isolated in man, which affects the skin, mucosa and various internal organs. It is caused by various species of Candida, which is a yeast-like fungi that produce pseudohyphae. Speciation helps to understand the epidemiology of Candida species particularly, the source and mode of transmission of resistant pathogens. Various commercially available chromogenic agar medium has been studied and evaluated for presumptive identification of various species of Candida. The present study was conducted for a duration of 12 months from the month of July 2019 to the month of July 2020, in the Department of Microbiology at a medical college in Siddipet, with prior approval of institutional ethics committee. The present study was aimed at isolating and identifying the Candida species from various clinical samples by using chromogenic media for easy and rapid speciation in addition to the time consuming and labour-intensive conventional methods. Among the Candida isolates the most frequently isolated species was found to be Candida albicans. In the present study non-albicans Candida (NAC) (50.91%) had predominance over Candida albicans (49.09%). In our study, an increase in the number of cases caused by NAC was noted though the most common species isolated was Candida albicans. CHROMagar was found to be a simple, easy and also a rapid method for Candida species detection. It considerably reduced the turn-around-time.

Introduction

Candidiasis is worldwide in distribution, and is one of the common fungal diseases isolated in man, which affects the skin, mucosa and various internal organs. It is caused by various species of Candida, which is a yeast-like fungi that produce pseudohyphae. (Apurba S Sastry, Essentials of Medical Microbiology, 3rd Ed) The genus Candida belongs to Phylum: Imperfectii, the Order Moniliales and family Cryptococcaceae. (Chander J. Candidiasis. In: A textbook of Medical Mycology, 3rd Ed.) Candida is a human commensal, but it becomes an opportunistic pathogen because of any pre-disposing factors which impair, immune response to the microorganisms. eg: AIDS, immunosuppressive chemotherapy, metabolic diseases, or cause an imbalance, in favour of fungal microflora e.g., Antibiotics, disrupt the integrity of the integument e.g., intravenous catheters, surgery. The source of infection is mostly endogenous, but in some cases, Candida can be introduced by exogenous sources too (Esther Segal and Daniel Elad. Candidiasis. Topley and Wilson’s Microbiology and Microbial Infections. Medical Mycology. 10thEd.) Fungal infections, especially those caused by Candida species, has significantly increased, in the past decade, in immuno- compromised patients. (Dharmeswari T., 2014)

The conventional method of fungal culture on SDA is tedious and often isolation and detection are difficult in mixed cultures. This led to the use of many chromogenic agar which enables the detection based on colour of the colony. (Baradkar VP, 2010; Moyer GJ, 1995; Murray MP, 2005; Louwagie B, 1995; Odds FC, 1994; Pfaller MA, 1996; Raut SH, 2009). Speciation of various species of Candida is based on the colour of the colony along with other characteristic. This differentiation is facilitated by the presence of chromogenic substrates that produce different pigmentations based on specific enzymes produced by the specific candida species. (Lynn L., 2003)

CHROMagar Candida is of great use in clinical specimens suspected to contain yeast and hence can be used as a medium for primary isolation even in a resource limited setting as it requires less expertise. Moreover, it can act as a differential medium even if candida is isolated from other media like SDA or blood agar. (Odds FC, 1994) Though the biggest limitation of the medium could be the cost but the advantage in reducing the turn-around time can still be of great significance when compared to various conventional methods of identification.

Speciation helps to understand the epidemiology of Candida species particularly the source and mode of transmission of resistant pathogens. (Shaheen M.A, 2006) Conventional methods for speciation are more time consuming and laborious, therefore, in the present study CHROMagar has been used for rapid identification of various species of Candida.

The present study was aimed at isolating and identifying various Candida species from clinical samples by using chromogenic media for easy and rapid speciation in addition to the time consuming and labour-intensive conventional methods.

Source : Phenotypic identification of Candida species from various clinical samples in a resource limited setting

[webionaire]

Rudolf Fischer's concept of ‘chromogenic development’ of sensitized silver halide, which used only one colour developer for producing the triad of subtractive primaries yellow—magenta—cyan in the presence of dye-forming substances called ‘couplers’, marked the starting point of the lengthy evolution that has generated a huge market for professional and consumer photography. The development of the colour-forming system has led to industrial products of high performance. This will be discussed in Section 1 with regard to its general aspects, as far as the years between 1960 and 2000 are concerned, and available sources, found mainly within the patent literature, can be evaluated.

[tmmediaindia]

PA E. Coli Kit: Water Quality Assurance Made Easy

Testing water has always been an essential part of our laboratory work. Whether it's testing a sample to see if it’s safe to drink or testing the purity in pharma labs, TM Media’s PA E. ColiKit, is an all-in-one product for the job. Let's see why this product is one of the best in water testing.

What Makes the PA E. Coli Kit So Special?

When we talk about water, we must understand that not all water is the same. Sometimes, you've got microbes, mostly coliform bacteria, living in the water, which makes it unsafe for use. The PA E. Coli Kit helps you figure out if these bacteria are causing trouble. It's a quick, budget-friendly solution that's also perfect for those off-the-grid spots where you might have doubts about the safety of water.

Inside the kit:

Providing everything in one place!

PA Medium: Main media for detection of microbial growth

Sterile PET bottle: To carry out the process in

Sterile poly bag: To discard

How Does It Work?

It’s as simple as it gets: add some water to the PET bottle, pour in the PA Medium, give it a good shake, and let it incubate at 35–37 °C. In 18–48 hours, if your mix turns yellow from it, you've got coliforms living in there.

How does it do that?

It's like this kit has everything you need in it. It follows two key rules:

No coliform bacteria should be present in 100 mL of drinking water.

If even one of these microbes is around, it will start a reaction, ferment lactose, and start producing acid and gas.

So, the PA Broth contains lactose and a pH indicator. If lactose is fermented, it'll change colour from the original purple to a vibrant yellow.

Spotting the real from the fake:

With this kit, there's no second-guessing. Different bacteria will make the medium change to specific colours, helping you spot exactly who’s in your water.

Like Escherichia coli, it will have luxuriant growth, and the colour will change to yellow. S. serotype typhimurium will have a turbid purple colour.

That’s not it. TM Media also provides you with various other water testing products for the analysis of water, like the Chromogenic Coliform Agar Plate (TMP 1858), which is ready to use.

To check our product list, click on the link

[laurad05]

Post-teeth whitening diet: what to avoid and what’s safe to eat

After teeth whitening, it’s crucial to be mindful of your food and drink choices for the first few days. Certain foods possess the potential to stain teeth or trigger sensitivity, making it prudent to avoid their consumption. This article delves into the specifics of which foods and beverages to exclude from your post-teeth whitening diet and provides insights into the safe alternatives.

Foods and drinks to avoid

1. Coffee and tea: We know it’s hard to resist your morning cup, but coffee and tea can be major culprits for teeth staining. The dark pigments they carry tend to cling to the porous enamel of your teeth, diminishing the impact of your recent teeth whitening.

2. Red wine: As enjoyable as a glass of red wine may be, its rich colour can leave unwanted stains on your newly whitened teeth. The tannins and chromogens present in red wine are notorious for leaving behind unsolicited stains, tarnishing the brilliance of your smile.

3. Berries: While delicious and nutritious, colourful berries like blueberries, blackberries, and raspberries contain pigments that can stain teeth.

4. Dark sauces: Sauces such as tomato sauce, soy sauce, and balsamic vinegar might be culinary essentials, but the chromogens contained in these sauces tend to latch onto enamel.

5. Dark chocolate: A piece of dark chocolate can be a real treat, but be mindful that this indulgence contains tannins that can potentially lead to discolouration.

6. Coloured beverages: It’s best to stay away from brightly coloured soft drinks, sports drinks, and artificially coloured beverages.

7. Citrus fruits: Citrus fruits might be good for you but they present challenges for freshly whitened teeth due to their acidic nature. The acidity can trigger heightened sensitivity, making it prudent to temporarily avoid them.

8. Dark leafy greens: Nutrient-dense dark leafy greens such as spinach and kale offer numerous health benefits, but their intense pigmentation could have a temporary impact on your teeth’s whiteness. While complete exclusion isn’t necessary, exercising caution in their consumption during this sensitive period is advised.

Other Foods to approach with caution:

While the above list outlines the most prominent culprits, it’s worth mentioning a few other foods that might warrant caution after teeth whitening:

1. Acidic Foods: Citrus fruits aren’t the only acidic foods to be cautious of. Pineapple, kiwi, and vinegar-based dishes should also be consumed in moderation to prevent sensitivity.

2. Spices: Vibrant spices like turmeric and curry can potentially stain teeth, so consider minimising their use during this period.

3. Pickled foods: Pickles and pickled vegetables can have strong colours that might impact your teeth’s whiteness temporarily.

4. Beets: While incredibly nutritious, beets can have intense pigmentation that might affect your teeth’s appearance.

Safe foods and beverages

During the critical post-whitening phase, it’s crucial to focus on foods and beverages that are less likely to stain your teeth or trigger sensitivity.

1. Water: Hydration is key. Water not only quenches your thirst but also helps flush away food particles that could contribute to staining.

2. Dairy products: Milk, cheese, and yogurt are low in pigments and can help neutralise acids in your mouth.

3. Lean proteins: Chicken, turkey, and fish are safe choices that won’t affect the whiteness of your teeth.

4. White grains: Opt for white rice and pasta, as they’re less likely to stain compared to their whole-grain counterparts.

5. Bananas: Bananas are a safe fruit option due to their lower staining potential.

6. Cauliflower: This mild-coloured vegetable is a versatile choice that won’t disrupt your teeth whitening progress.

7. Skinless potatoes: Enjoy potatoes without the skin to minimise potential staining.

8. White sauce: Cream-based sauces with a light colour can be enjoyed in moderation.

9. Clear broths: Clear soups and broths are gentle on teeth and won’t contribute to staining.

10. Clear beverages: Aside from water, clear herbal teas and coconut water can be enjoyed without worry.

By avoiding staining culprits and embracing teeth-friendly options, you’re taking proactive steps to preserve the brilliance of your newly whitened smile. Remember, the first 48 hours are pivotal, and as time passes, you can gradually reintroduce restricted foods while maintaining the sparkle of your smile.

[helvaticacare]

Cytokine Elisa Principle

The study of cytokines is useful in the investigation of inflammation. Cytokines are tiny proteins that convey information between cells and activate immunity in response to infection, inflammation, and other diseases. Accurate detection and measurement of cytokine concentrations are critical in characterising the nature of the infection and powerful in tracking illness progression.

Scientists are growing interested in enzyme labels and immunoassays that use enzyme-conjugated antibodies. The indirect sandwich enzyme-linked immunosorbent assay, or ELISA, is a low-cost analytical instrument used to analyse antibodies, antigens, proteins, and glycoproteins. There are numerous applications for cytokine analysis using ELISA, including those for neurological illnesses.

Helvetica Health Care (HHC) experts emphasise this significant medical application and how it aids in cytokine analysis.

What is elisa, and why is it used to detect cytokines?

The classic Sandwich ELISA test is a basic but extensively used instrument in medical laboratories throughout the world for detecting, measuring, and distinguishing a single cytokine from a mixture of biomolecules in any given sample.

ELISAs deliver specific, precise, and sensitive results, with the high-throughput rates required for cytokine protein analysis, whether the investigation is conducted in vitro or in vivo. In our whole blood assays, ELISA can typically assess cytokines produced in a culture medium, the concentration of ex vivo cytokine levels in plasma and serum, and triggered cytokine production.

Because it uses antibodies that are specific to a single cytokine or type, ELISA gives great precision. Sequential ELISA tests are used to evaluate several cytokines proteins from tiny samples.

How Does Elisas Function?

In principle, a basic sandwich ELISA analyses antigens between a layer of capture and detection antibodies. In other words, it is performed using an antibody-antigen-antibody sandwich. Below we explain the four steps of the simple indirect sandwich ELISA process:

1. Extracting analyte (specimen extracted for analysis) from a capture antibody sample.

2. Identifying biotin-labelled captured analyte with detection antibody (also specific for extracted analyte).

3. Detection amplification with streptavidin conjugated with an enzyme

4. Adding substrate and measuring the coloured signal via optical density (OD) using a microplate reader.

Scientists frequently use a microwell format (microwell plates) when conducting a traditional ELISA test.

Before we move on to a detailed explanation of the above steps, let us remind you that HHC provides a wide range of ELISA kits ready to use with break-apart wells. Our range of ELISA includes:

• The RETROTEK™ range is designed for the detection and quantitation of retroviral antigens from the retroviruses HIV-1, SIV and HTLV found in cell culture, serum, plasma or other biological fluids

• IMMUNOTEK™ kits can detect and quantify various immunoglobulins from many species, including Humans, Chicken, Cow, Goat, Rabbit, Rat and Mouse. We also provide HHV-6 IgG antibody and KSHV/HHV8 IgG antibody ELISA kits.

Describe the general elisa technique

Typically, the sample contains highly purified anti-cytokine antibodies, also known as capture antibodies, linked to an enzyme. Following plate washings, the immobilised antibodies are employed to capture the soluble cytokine proteins present in the applied samples. After washing the unbound material, biotin-conjugated anti-cytokine antibodies (detection antibodies) are utilised to identify the trapped cytokine proteins.

Following that is an enzyme-labeled avidin or streptavidin step. When a chromogenic substrate is introduced to the capture antibodies, it produces a signal that can be detected due to the substrate's colour change. The amount of coloured product produced by the bound, enzyme-linked detection reagents is simply quantified spectrophotometrically using an ELISA-plate reader at the appropriate optical density (OD). When the plate reader is connected to a computer, data storage and reanalysis are greatly facilitated.

A standard curve is introduced to a sandwich ELISA assay by serially diluting a standard cytokine protein solution with a preset concentration. Standard curves, also known as calibration curves, typically depict the standard cytokine protein concentration (usually ng or pg of cytokine/ml) vs the related mean OD value of duplicates. The concentrations of the potential cytokine-containing samples can be extrapolated from the standard curve.

The use of an ELISA computer application makes this operation easier. In general, completing a dilution series on the unknown samples helps to guarantee that the OD falls within the standard curve's linear range. The ELISA reagents used may have an impact on the curve fit analyses that researchers apply on their data, including either linear-log, log-log, or four-parameter transformations. 

Just like there are different types of cytokines, there exist other ELISAs procedures too:

· The Checkerboard method for optimising antibody concentrations

· The Dose-Response method for optimal blocking and dilution buffer for the sample matrix

· The Standard ELISA method for determining an analyte’s concentration in a given sample

· The Sequential ELISA

· The Multiplex ELISA

This fundamental approach can be improved by using sequential ELISA to test multiple analytes from a single sample aliquot. In this situation, a single sample is removed from one ELISA plate and then incubated in a different plate because the first plate would only catch the cytokine recognised by the antibody used for cytokine detection.

Multiplex ELISA is an excellent alternate method to the sequential ELISA wherein numerous capture antibodies are printed into a single microplate well, each with a different set of specificities.

Contact us at our Geneva office to inquire about the availability of our ELISA kits.

[pearlywhitebleachingwhitening]

What is Teeth Whitening?

Your teeth can obtain tarnished gradually, mainly due to the food and drinks we consume. The colour pigments in foods and also drinks like coffee, tea and merlot bind to the surface area of your tooth enamel. These colours are known as chromogens and make your teeth show up darker than they really are. Teeth Lightening is a cosmetic dental procedure that can get rid of these stains and also leave you with a whiter smile. This kind of therapy is popular as well as an increasing number of people are seeking it out. The ADA suggests that you speak with your dental professional prior to going through any kind of type of teeth whitening therapy. This will enable you to prevent possible side effects as well as take full advantage of the effectiveness about your bleaching outcomes.

There are a number of over-the-counter (OTC) and in-office teeth bleaching treatments that use bleaching representatives to lighten intrinsic and extrinsic spots on the teeth. These oxidizing agents, including hydrogen peroxide and also carbamide peroxide, permeate the teeth to damage down the staining while not softening or thinning the teeth. When made use of correctly, a professional-grade whitening remedy will certainly supply dramatic results. We'll use a protective guard to your gums and afterwards provide a highly concentrated bleaching agent straight onto your teeth. This bleaching process will certainly target the deepest layers where staining starts to provide you that "excellent" smile you have actually constantly desired. Before undertaking teeth bleaching, we'll assess your smile and also aid you determine what stains require to be gotten rid of. Our dentist at this site will likewise be able to recognize whether the discolorations you're looking to whiten are inherent or external and the number of gos to will certainly be needed to attain your wanted end result. Our goal is to develop a bleaching service that will certainly assist you have a brighter, extra stunning smile permanently.

We will certainly personalize a therapy plan for you and ensure that the whitening treatment is safe, effective, economical, and hassle-free. We know that tarnished teeth can have a negative impact on your self-esteem and also confidence, so we enjoy to offer our individuals the choice of whitening their teeth at our Narberth,  workplace. Our in-office teeth bleaching procedures will certainly brighten your smile by several tones as well as will make certain to improve your dental health as well! Utilizing a tooth paste for sensitive teeth a few weeks prior to your whitening visit will assist maintain your teeth and gums safeguarded from the peroxide. If you do experience sensitivity after your lightening, it is typical as well as should decrease on its own.

To keep a healthy, bright smile, we advise adhering to a few straightforward rules: 1. Don't consume or smoke any discoloration drinks 2. Stay away from foods and beverages that will certainly continue to create discoloration on your teeth 3. Brush twice a day with an ADA-approved lightening tooth paste. Your smile is a reflection of your overall self-confidence as well as happiness. It can have a substantial impact on your social as well as expert lives. Studies have revealed that a person who has a whiter, more attractive smile is most likely to be hired as well as dealt with more positively than an individual with a less than ideal smile. Discover more facts about dentist at http://kids.britannica.com/comptons/art-73293/An-orthodontist-works-on-a-patients-braces.

[asiawalecka]

Visual postcards from Masada, Dead Sea, Israel 8102

120mm

[afrouif]

Louise Lawler

Marie +270, 2010-12

Chromogenic colour print

149.9 x 115.6 cm

The Museum of Modern Art, New York

[gliklofhameln]

God Is In Our Clubs

Tomer Ganihar

Israeli, b. 1970

1996

Chromogenic colour print mounted on aluminum

[fernpapst]

Kohlscheid 1981, vintage chromogenic colour print, 22.9 x 30.0 cm, unique, Collection Centre Canadien d'Architecture