#Endonuclease
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#biobasic#labexperiments#DNase#RNase#Protease#Endonuclease#researchers#perfect#solution#ultrapurewater#research#industry#standards#experiments#safety#compliance
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trying to do my biology homework but all i can think about is dan and phil shop... more like phorward phrimer im losing my mind.
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ARP genes function, at least in part, by helping maintain the repression of KNOX1 (KNOTTED1-LIKE HOMEOBOX) genes in the developing leaf (Figure 19.5A). (...) Expression of the HD-ZIP III genes, such as PHABULOSA (PHB), and PHAVOLUTA (PHV), is normally limited to the adaxial domains of the leaf primordia (see Figure 19.5A). (...) The expression of miR166 in abaxial regions of the leaf primordia has been shown to reduce PHB and PHV transcript levels, thus enabling normal abaxial patterns of development (Figure 19.5B). (...) KANADI genes and HD-ZIP III genes play antagonistic roles in adaxial-abaxial patterning in both leaves and vasculature (see Figure 19.5B). (...) In Arabidopsis, expression of YABBY genes marks the abaxial domain and marginal regions of primordial leaves (see Figure 19.5A). (...) YABBY transcription factors positively regulate a member of the WOX gene family, PRS (PRESSED FLOWER), which is expressed in the leaf margin and promotes blade outgrowth (see Figure 19.5B). (...) PRS- and WOX1-dependent blade outgrowth is, in part, mediated by an as yet unidentified mobile signal(s) processed by KLU, a cytochrome P450 monooxygenase (see Figure 19.5B). (...) Developing leaf primordia can be divided lengthwise into four main zones extending from the meristem: boundary meristem, lower-leaf zone, petiole, and blade (see Figure 19.5A). (...) The region of the leaf primordium destined to become the petiole is characterized by the expression of BOP (Blade on Petiole) genes, which encode transcriptional activators that are required to establish petiole identity in the proximal portion of the leaf in Arabidopsis (see Figure 19.5A). (...) This polarity results in the differentiation of xylem on the adaxial side of the leaf vein, and phloem on the abaxial side (see Figure 19.5).
"Plant Physiology and Development" int'l 6e - Taiz, L., Zeiger, E., Møller, I.M., Murphy, A.
#book quotes#plant physiology and development#nonfiction#textbook#knox1#knotted like homeobox#arp#apurinic endonuclease redox protein#leaves#hd zip iii#phabulosa#phb#phavoluta#phv#mir166#microrna#kanadi#leaf veins#vascular leaves#yabby#arabidopsis#wox#wuschel homeobox#prs#pressed flower#wox1#klu#cytochrome#bop#blade on petiole
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send me asks? perhaps? if you feel like?
#losing my mind and my entire sanity over exam week#i havent slept in so long that time feels like its endless but also over in a blink#like that odd little ball of timey wimey stuff yk?#anyway#asks to distract the ole brain from restriction endonucleases and calvin cycles perhaps?#love yall#hope i come out of this sane#sarah rambles#midnight musings
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that's right baby it's that "this is definitely for an audience of 3 people total" galetash modern au ficlet. ~1.2k, T-rated, just a bit of conversation :)
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What’s the best molecule out there?
Anon. I'm convinced you're actually trying to kill me. I thought so hard for so long that I gave myself a headache 💀 (the trying to kill me is a joke, but I did give myself a headache, most likely from dehydration tho)
Least favourite is easy tho; citric acid (f that shit)
I love the Cas9 endonuclease (part of CRISPR/Cas) because of all the great opportunities it theorethically gives us. It's also just cool that bacteria have what's essentially an immune system.
Moronic acid is also a good one (because of the name) which is naturally found in mistletoe and sumac. It's also used as an antiviral agent for things like herpes simplex virus and HIV
Rag recombinase is also great! That's part of our immune system and is what allows our adaptive immune system to rearrange the genetic material of T and B cells to create a potential weapon against any disease
I could go on....
#sorry anon but anyone who gets me started with questions like that will suffer#screaming at the murder
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ngl kinda pissed off with the way the world works like you spend your first 10 20 years just learning learning learning:
when you draw, by hand, a graph and it has an asymptote, you must not in any way indicate that the line diverges or moves away from the asymptote. the formula for calculating temperature loss in an environment!! that was my favourite :<
nutrient agar would be described as a control, a negative control to be precise because in this instance, no growth is expected. a "lawn" of bacteria in a Petri dish is when all individual colonies in an agar plate merge to form a field, or mat, of bacteria
Gel electrophoresis of DNA. endonucleases (restriction enzymes) hydrolyse (cut) the phosphodiester bonds at specific DNA base pair sequences. In the bacteria, the restriction enzymes cut DNA as a protective mechanism against invading foreign DNA. smaller fragments can move faster through the agarose matrix from the cathode to the anode, even though the larger fragments (i.e., 23kb) are more electronegative.
if animals are stressed before slaughter, you may end up with either PSE (pale, soft, exudative - severe short term stress) or DFD (dry, firm, dark - longer term stress). This is because they either suffer a rapid breakdown of muscle glycogen (PSE), or their muscle glycogen is used up during handling, transport, before and after slaughter (DFD).
the literary devices employed by the author work in tandem to elicit an emotional response from the reader by appealing to their sense of humanity, as well as an imagined psychological trauma.
data can be stored on a hard drive next to each other in physical space and we call this contiguous. It's useful for certain data structures, sometimes necessary. But you may not have enough free memory to access or execute programs if it needs to be contiguous. This is where something like a linked list data structure can come in handy.
Metamorphic rocks are are those that have been altered by external forces, such as (and typically) pressure and temperature. Eluviation is the process of clay leaving the A1/A2 horizons and heading toward the B horizon. Illuviation is clay accumulating into the B horizon. Leaching is just the movement of other things like phosphate, nitrates, etc, downward toward bedrock. The triangular soil texture (clay/silt/sand) diagram!
K(S) + H2O(I) → H2(g) + KOH (no idea what this even meant tbh)
I used to know all of that, and more, all at once. But now here I am filling out forms for people and scanning their documents and liaising with insurance, medical, financial, and other companies on their behalf.
"Why am I learning trig? When will we ever need this?" truth is little Timmy, you (on average) won't get to use it, you (on average) won't experience the joy of using these magnificent tools we get to learn at a young age, you (on average) will be robbed of every opportunity to experience this magic.
So. Enjoy it...
#tech#capitalism#codeblr#studyblr#biology#science#ecology#environmental science#soil science#agriculture#chemistry#agriblr#chemblr#biolblr#are any of these tags valid?#oh yea#mathblr#math
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Human’s inherent desire for understanding, and why angels are a perfect lure. (Rambling)
Humans have studied the art of the mystic for centuries. Before science, literature, and math, there were stories. Because storytelling is what guides us to experience, to learn, to make sense of both experience and knowledge.
Even when we do science, we say: “First, extraction of the sample DNA from the flesh was conducted through the process of centrifuge. Then, PCR was run to amplify the amount of recovered DNA. Restriction endonuclease enzyme was added to the sample, fragmenting DNA into smaller strands. The product was evaluated through agarose gel electrophoresis. 80-150V of electric force pulling the pieces toward the bottom. The shorter the pieces are, the faster they go. So, the DNA separates more, and paints a ladder of bands. You cannot see them. As the last step, you must stain them with fluorescent dye, and only under UV lights can you observe the crude data.”
Temporal. Sequential. Meaningful. This is a story called “DNA fingerprinting”.
The story of magic and godly realms and religion is of the same. They carry teachings (and entertainment). They last through centuries because there is something in them that humanity sees.
Humans are driven by a maddening sense of curiosity and exploration. To make sense of it all. To separate organs from man, to separate cells from organs, to separate DNA from cells, and to do it again, at a smaller scale with enzymes. There is an inherent desire to learn until all is deprived. To become passionate is to be consumed wholeheartedly.
So we sent people to explore the Arctic, the ocean, the sky, the universe. And when they perish, we send more.
The study of death is the same. To see beyond the veil is something impossible, because the dead cannot return. (Well, they technically can, depending on how you define death. If death is the stopping of the heart, then I suppose we are dying, in microdoses, every second of our lives. If death is the cease of memory and autonomy, then I suppose we are dying, in microdoses, every night in our beds.)
(I digress.)
The study of death is attractive because it looks into what we are sure we cannot possibly touch. So we only hope to examine what we can. The maggots that gnaw at the meat, the stillness of limbs in silence, the invasive infestations of bacteria and mold and creatures of all kinds.
The corpse is an afterimage of an experience of both life and death. We can only hope to study the husk and the life that sustains on that husk, hoping it is close enough to touch death.
It is similar to the study of the supernatural in that way. Magic only exists because we do not understand it. That’s why it is so captivating. The creation of a potion in a cauldron is the same as biochemistry. The transformation of forms and elements is the same as fusion physics. The impossible feats of flight were achieved by aeroplanes and carefully measured aerodynamics. There are ghosts born from boring undetected monoxide poisoning.
When we understand, magic loses its… well, magic.
It is similar to the study of religion in that way. Because we are desperately lonely, and we must make meaning, and so magic shall suffice in place of what we do not know and to fill what we do not have. I do not study religion, but I know at least a part of this is true – at least in its origin. The stories of gods, angels, demons, palaces in the sky, monsters in the ocean, a form of thousand eyes and arms and all-knowing and all being and loves like nothing else because we are greedy organisms that crave validation and safety and love and love and love. And we can learn anything it wants us to learn, make it through anything if love and peace are waiting for us at the end of it all. (Though religion, in all its implications, forms, and renditions have changed since then, as well as the interpretations of survived passages.)
I am not a believer in a higher being, nor am I a student of religion, so I cannot speak of all of it. I cannot claim understanding.
I think this is also partially why angels compel me so. They are the beyond. Above reasoning, above logic, in the same realm as the untouchable pureness of undiscovered science, death, magic, and religion.
What stories flow within its (his?) veins? What stories lie dormant in its (his) throat? What stories are etched on the body, the wings, the blade? What stories speak of the beating of its (his) heart and the bleeding of its (his) light? What of the cells, the molecules, the very physics (magic) that binds it (him) together?
Do you speak of the stories of love and despair and violence and hope as we do?
Please, do not answer me.
Because to know is to kill. The utter destruction of the imagination and wonder and passion. To purposefully look away from knowledge is the complete comprehension that understanding makes something die. It brings dullness to love.
So, please, let me see you in my mind’s eye, and nothing more.
#az thoughts#angelcore#rambling again and has to get this out of my body#yea its bc gabriel got me thinking again#long post#writing#spilled ink#<- recently learned this tag exists#im a fan of a few really strong lines but this is honestly a bit tedious to read#if you're reading i really hope you enjoyed lol#az personal
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started genetics class this fall. "histone acetylation generally destabilizes chromatin structure and is associated with an increase in transcription" "when the Dmnt3 gene in Apis mellifera is silenced the genes encoding queen bee traits remain unmethylated and produce a queen bee phenotype" "restriction endonucleases recognize specific nucleotide sequences in DNA and make double-stranded cuts at those sequences" i am being seduced by a fucking textbook
#ALSO!! got some amazing things going on that i refuse to elaborate on until i (hopefully) receive an acceptance letter on monday#but its amazing stuff and im off my rocker with excitement#cannot even PRETEND to be chill#buggie's nerd stuff
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*Gasp* You take that back! E(scherichia) coli is the most beautiful organism on this god-damn planet! God made E-coli and the rest of us are here for its benefit, the face of god is a rod shaped gram-negative bacterium. Sure it kills a few people every year. It can have that, as a treat. E-coli recombinant dna oiukqjgwiueyudiwouiluhkniueqwenoyui I live for the computer's protein models that I spent 3 hours having swiss model render, all from e-coli gene sequences. e-coli is where we get a clear idea of the mechanics and structure of the best enzyme in all living things! look at it's well understood metabolic pathways! look at it's beautiful circular DNA, look at it's prokaryotic cell structure, at it's v-atpase, it's plasmids it's endonucleases. Fucking model organism. I will not allow E-coli slander on this blog
e(vil) coli
#biology#shitpost#kind of#but also E-coli is literally considered the model organism and does all the things I mentioned above#E-coli is responsible for all synthesized protein#like insulin
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Cutting-Edge CRISPR: Latest Advances in Genome Editing Technologies
CRISPR-Cas9 technology has revolutionized the field of genome editing since its introduction, offering unprecedented precision and ease in altering DNA sequences. This powerful tool has enabled researchers to explore genetic functions, develop therapies for genetic disorders, and even consider applications in agriculture and environmental conservation. As CRISPR technology continues to advance, new methods and improvements are emerging, pushing the boundaries of what genome editing can achieve. This article explores the latest developments in CRISPR technology, highlighting their implications and potential for future applications.
Beyond Cas9: Expanding the CRISPR Toolbox
While Cas9 has been the most widely used enzyme in CRISPR technology, researchers are now exploring other CRISPR-associated proteins, such as Cas12a (Cpf1), Cas13, and Cas14. These enzymes offer unique properties that can be advantageous for specific applications. For example, Cas12a creates staggered cuts in DNA, which can be useful for certain types of gene editing, while Cas13 targets RNA instead of DNA, opening up possibilities for manipulating gene expression without altering the genome itself.
The discovery and characterization of these new CRISPR systems expand the toolbox available to scientists, enabling more tailored and efficient genome editing strategies. For instance, Cas12a’s ability to process its guide RNAs autonomously simplifies the design of multi-gene editing experiments. Similarly, Cas13’s RNA-targeting capabilities hold promise for treating diseases caused by aberrant RNA, such as certain neurological disorders.
Prime Editing: Precision Redefined
Prime editing represents one of the most significant recent advancements in CRISPR technology. Developed as a more precise alternative to traditional CRISPR-Cas9 editing, prime editing allows scientists to directly write new genetic information into a DNA sequence without causing double-strand breaks. This technique uses a modified Cas9 enzyme fused to a reverse transcriptase enzyme and a specialized guide RNA known as a prime editing guide RNA (pegRNA).
The precision of prime editing reduces the likelihood of off-target effects, making it a safer option for potential therapeutic applications. Moreover, prime editing can correct a wider range of genetic mutations, including all possible base substitutions, small insertions, and deletions. This capability makes it a versatile tool for treating genetic diseases, potentially offering cures for conditions that were previously difficult or impossible to address with earlier genome-editing technologies.
Base Editing: A Subtle Yet Powerful Approach
Base editing is another breakthrough in genome editing that allows for the precise conversion of one DNA base into another without introducing double-strand breaks. This method utilizes a modified Cas9 enzyme that nicks one strand of the DNA, coupled with a deaminase enzyme that chemically alters the targeted base. Base editing has proven particularly useful for correcting point mutations, which are responsible for a significant proportion of genetic diseases.
The subtleness of base editing reduces the risks associated with more invasive genome-editing techniques, making it a promising tool for clinical applications. Recent advancements in base editing have improved its efficiency and expanded its applicability to a broader range of genetic contexts. Researchers are now exploring its use in treating conditions like sickle cell disease, cystic fibrosis, and muscular dystrophy.
CRISPR in Diagnostics: Beyond Genome Editing
While CRISPR is primarily known for its genome-editing capabilities, its potential applications extend beyond editing DNA. CRISPR-based diagnostic tools, such as SHERLOCK (Specific High-sensitivity Enzymatic Reporter unLOCKing) and DETECTR (DNA Endonuclease Targeted CRISPR Trans Reporter), are being developed to detect nucleic acids with high sensitivity and specificity. These tools harness the RNA-targeting properties of Cas13 or the DNA-cleaving abilities of Cas12 to detect the presence of specific genetic sequences, making them powerful tools for diagnosing infectious diseases and genetic disorders.
These CRISPR-based diagnostics are highly accurate and relatively easy to use and cost-effective, making them suitable for point-of-care testing in various settings. As the technology continues to evolve, CRISPR diagnostics could become a standard tool in clinical laboratories and remote healthcare environments, offering rapid and accurate detection of pathogens, genetic mutations, and other biomarkers.
Ethical Considerations and Regulatory Challenges
As CRISPR technology advances, it brings with it significant ethical and regulatory challenges. The ability to edit the human genome, particularly germline editing, raises concerns about the potential for unintended consequences, such as off-target effects or the creation of designer babies. The use of CRISPR in agriculture and the environment also poses ethical questions about the long-term impacts of genetically modified organisms (GMOs) on ecosystems and biodiversity.
Regulatory bodies around the world are grappling with how to oversee the use of CRISPR technology while balancing the need for innovation with safety and ethical considerations. As new CRISPR-based therapies and products move closer to commercialization, it will be essential to develop comprehensive guidelines that address these challenges while fostering responsible use of the technology.
CRISPR and Agriculture: Engineering a Sustainable Future
CRISPR technology is not limited to medical applications; it is also being used to revolutionize agriculture. By enabling precise genetic modifications, CRISPR allows scientists to develop crops that are more resistant to pests, diseases, and environmental stressors. This has the potential to improve crop yields, reduce the need for chemical pesticides, and enhance food security.
One of the most promising applications of CRISPR in agriculture is the development of crops that can withstand the effects of climate change. For example, researchers are using CRISPR to create drought-resistant crops that can thrive in arid conditions, as well as plants that can absorb more carbon dioxide from the atmosphere, helping to mitigate the impact of global warming. As CRISPR technology continues to advance, it will likely play a crucial role in creating a more sustainable and resilient agricultural system.
Future Directions: Where CRISPR Is Heading
The future of CRISPR technology is filled with possibilities. Researchers are exploring ways to improve the efficiency, specificity, and versatility of CRISPR systems, potentially expanding their applications even further. One area of active research is the development of CRISPR systems that can target and edit multiple genes simultaneously, which could be used to study complex genetic networks and develop more comprehensive treatments for multifactorial diseases.
Another exciting direction is the integration of CRISPR with other emerging technologies, such as artificial intelligence and nanotechnology. AI could be used to predict the outcomes of CRISPR edits more accurately, while nanotechnology could enhance the delivery of CRISPR components to specific cells or tissues in the body. These innovations could make CRISPR even more powerful and accessible, paving the way for new breakthroughs in medicine, agriculture, and beyond.
In Conclusion
CRISPR technology has come a long way since its introduction, and the latest advances are pushing the boundaries of what genome editing can achieve. From the development of new CRISPR-associated proteins and precise editing techniques like prime and base editing to the expansion of CRISPR’s applications in diagnostics and agriculture, the potential of this technology is vast. However, as CRISPR continues to evolve, it will be crucial to address the ethical and regulatory challenges it presents to ensure its responsible and beneficial use. The future of CRISPR is bright, and its impact on science and society is only just beginning to unfold.
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i am fucking tired of all the idiots going "WAAA EUGENICS" every fucking time the word DNA comes up do none of you fucks know about biotechnology? gene editing? restriction endonucleases like Hind Ⅱ and EcoR Ⅰ? cloning vectors like pBR322? agarose gel electrophoresis? ethidium bromide? do none of these words jog your memories of school? gene therapy? Hb S gene causes sixth position of the beta globin chain substituted with valine causing sickle cell anemia?
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Nuclease P1 from Penicillium citrinum
Nuclease P1 from Penicillium citrinum Catalog number: B2017808 Lot number: Batch Dependent Expiration Date: Batch dependent Amount: 1 Vial Molecular Weight or Concentration: N/A Supplied as: Powder Applications: a molecular tool for various biochemical applications Storage: 2-8°C Keywords: 3′-Phosphohydrolase, Nuclease 5′-Nucleotidehydrolase, Endonuclease P1 Grade: Biotechnology grade. All…
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Restriction Endonucleases Market Size, Share, Emerging Factors, Trends, Segmentation and Forecast to 2030
Market research “Restriction Endonucleases Market Size, Share, and Growth by 2031” enriched with data tables, pie charts, figures, and graphs spread through chapters reveal actionable insights. At present, the Restriction Endonucleases market is expanding at a lucrative CAGR. Through this assessment, The Insight Partners attempts to predict future trends, market values, growth factors, and related statistics. The report incorporates a broad range of strategies such as acquisition, collaborations, and investigation are embraced by market players to stay ahead in the competitive Restriction Endonucleases market space.
This market research is enriched with key statistics and facts allowing manufacturers to devise further business strategies. The market report also offers the company landscape and corresponding details of major market participants. The data contains company profiles, yearly turnover, product launches, income sources, and acquisitions.
Restriction Endonucleases market share has grown at a lucrative rate in recent years. Various factors that determine Restriction Endonucleases market growth is examined in this report, including opportunities, barriers, challenges, trends, and drivers. Authentic market determinants encourages innovation. This section addresses the distribution of firm activity and the factors that influence development. A comprehensive range of market-specific data is available, allowing investors to conduct an early assessment of the Restriction Endonucleases market's capabilities.
The main aim of the Restriction Endonucleases market report is to present an unbiased evaluation of the market based on industry growth potential, recent developments, trends, and growth opportunities. A detailed report is structured in a way such that users will find it easy to navigate and understand. We have ensured the optimal use of visual representations wherever necessary. This has increased pictorial presentation and the advantage of easy interpretation of industrial facts.
Scope of Restriction Endonucleases Market Research Report
Restriction Endonucleases Market size and forecast at global, regional, and country- level for all the key market segments covered under the scope
Market dynamics such as drivers, restraints, and key opportunities
Key future trends
Detailed PEST and SWOT analysis
Global and regional market analysis covering key market trends, key players, regulations, and recent market developments
Industry landscape and competition analysis covering market concentration, heat map analysis, key players, recent developments
Detailed company profiles
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Detailed historical data analysis, and market size forecast
Key market drivers influencing market growth
Emerging trends and opportunities in Restriction Endonucleases market
Analysis of major players to understand their strategies
Examination of regional dynamics
Report Attributes
Details
Segmental Coverage
Type
Type I
Type II
Type III
Type IV
Others
Application
Polymerase Chain Reaction (PCR)
Restriction Fragment Length Polymorphism (RFLP)
Epigenetics
Restriction Digestion
Sequencing
Cloning
End User
Hospitals
Clinics
Academic Research Institutes
Pharmaceutical and Biotechnology Companies
Diagnostic Centers
Geography
North America
Europe
Asia Pacific
and South and Central America
Regional and Country Coverage
North America (US, Canada, Mexico)
Europe (UK, Germany, France, Russia, Italy, Rest of Europe)
Asia Pacific (China, India, Japan, Australia, Rest of APAC)
South / South & Central America (Brazil, Argentina, Rest of South/South & Central America)
Middle East & Africa (South Africa, Saudi Arabia, UAE, Rest of MEA)
Market Leaders and Key Company Profiles
New England Biolabs
ThermoFisherScientific
Takara Bio Inc
Illumina
Agilent Technologies, Inc
F. Hoffmann-La Roche Ltd
NIPPON GENE CO., LTD
Promega Corporation
Merck KGaA
Jena Bioscience GmbH
Other key companies
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The following are some customizations our clients frequently ask for:
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Restriction Endonucleases #biology #molecularbiology #science #genetics...
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