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Sodium Salt salt CAS:139-41-3 Manufacturer Price
N,N-Bis(2-hydroxyethyl)glycine sodium salt is a chemical compound used as a buffering agent in various biochemical and biophysical applications. It helps maintain a stable pH level in experimental conditions, making it useful in enzyme studies, protein research, cell culture, and Western blotting techniques.
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4-Aminophthalhydrazide AMPPD CAS:3682-14-2
4-Aminophthalhydrazide, also known as 4-APhH, is a chemical compound with the molecular formula C8H8N2O. It belongs to the class of hydrazide compounds and is derived from phthalic acid.
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2-Chloro-4-nitrophenyl-α-L-fucopy ranoside CAS:157843-41-9
2-Chloro-4-nitrophenyl-alpha-L-fucopyranoside is a synthetic chemical compound. It is a derivative of fucose, a monosaccharide that is commonly found in various biological molecules. This compound contains a chlorine atom and a nitro group attached to a phenyl ring, which is linked to the fucose molecule.The specific applications and properties of 2-chloro-4-nitrophenyl-alpha-L-fucopyranoside may vary, depending on its intended use. However, similar fucoside derivatives have been used in biochemical research for various purposes, including studying glycosylation processes, investigating enzyme activities, and analyzing carbohydrate-protein interactions.
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Guanidine Hydrochloride CAS:50-01-1
Guanidine hydrochloride is a chemical compound with the molecular formula CH5N3·HCl. It is a strong chaotropic agent widely used in biochemistry and molecular biology applications.
Guanidine hydrochloride is commonly used to denature proteins, disrupt protein structures, and unfold proteins for purification purposes. It is particularly effective in breaking hydrogen bonds and disrupting non-covalent interactions within proteins. This property makes it useful for solubilizing proteins that are normally insoluble or aggregate-prone.
It is also utilized as a protein stabilizer, protecting proteins from unwanted aggregation or denaturation during various biochemical and biophysical experiments. Guanidine hydrochloride can help maintain the native structure and activity of proteins under denaturing conditions.
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NSP-AS CAS:211106-69-3 Manufacturer Price
The compound 3-[9-(((3-(carboxypropyl)[4-Methxylphenyl]sulfonyl)aMine)carboxyl]-10-acridiniuMyl)-1-propanesulfonate inner salt is a complex molecule consisting of an acridinium moiety attached to a propanesulfonate inner salt. It contains a carboxypropyl group, a 4-Methxylphenylsulfonyl group, and an amine group. This compound is likely synthesized for specific applications in areas such as chemistry, pharmaceuticals, or research.
Furthermore, NAC has shown promise in supporting liver health by assisting in the removal of toxic substances, such as acetaminophen, a common pain reliever. It may also have protective effects against liver damage caused by alcohol consumption.
In addition to its antioxidant and respiratory support properties, NAC has been explored for its potential benefits in mental health. Some research suggests that it may have a positive impact on mood disorders, such as depression and obsessive-compulsive disorder (OCD).
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BCIP-Toluidine)5-Bromo-4-chloro-3-indolylphosphate-p-toluidine salt CAS:6578-06-9
BCIP-Toluidine, also known as 5-Bromo-4-chloro-3-indolylphosphate-p-toluidine salt, is a chemical compound commonly used in molecular biology and biochemistry research. It is primarily used as a substrate in enzyme-linked immunosorbent assays (ELISAs) or immunohistochemical staining techniques to detect alkaline phosphatase activity.
When BCIP-Toluidine is cleaved by alkaline phosphatase, it undergoes a color change reaction, producing a blue-purple precipitate. This reaction allows for the visualization and quantification of alkaline phosphatase activity in samples. The intensity of the color can be measured spectrophotometrically and is directly proportional to the enzyme activity.
The use of BCIP-Toluidine as a substrate is especially common in applications involving DNA or RNA labeling, such as in situ hybridization (ISH) or Southern and Northern blotting. It provides a reliable and sensitive method for detecting the presence of target nucleic acids in samples.
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b-D-Glucopyranoside,2-chloro-4-nitrophenyl 2-(acetylamino)-2-deoxy- CAS:103614-82-0
2-chloro-4-nitrophenyl-N-acetylglucosaminide is a chemical compound that belongs to the family of N-acetylglucosamine derivatives. It is commonly used as a substrate in enzymatic assays to measure the activity of certain enzymes, such as glycosidases and glycosyltransferases.
The compound has a molecular structure consisting of a N-acetylglucosamine moiety, which is a derivative of glucose, and a 2-chloro-4-nitrophenyl group attached to the sugar molecule. The presence of the 2-chloro-4-nitrophenyl group makes this compound highly sensitive to enzymatic cleavage by glycosidases, resulting in the release of the 2-chloro-4-nitrophenol molecule. The amount of released 2-chloro-4-nitrophenol can be quantified through spectrophotometric measurements, allowing for the determination of enzyme activity.
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![N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly CAS:64967-39-1](https://cdn.globalso.com/xindaobiotech/图片478.png)
N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly CAS:64967-39-1
N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly is a chemical compound with a complex name that represents a specific peptide sequence. It consists of various amino acids connected together in a specific order: phenylalanine (Phe), glycine (Gly), and glycine (Gly).
The compound is modified with a furan ring at the acryloyl group, which gives it unique properties and functions. This modification may impart unique characteristics to the compound, such as altered stability, reactivity, or biological activity.
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4,5-Diazafluoren-9-one CAS:50890-67-0
4,5-Diazafluoren-9-one is a chemical compound that belongs to the class of heterocyclic aromatic compounds. It consists of a fluorene skeleton with two nitrogen atoms (diaza) and an oxygen atom (one) attached at specific positions. It is commonly used as a building block or intermediate in organic synthesis, especially in the preparation of various organic compounds, pharmaceuticals, and dyes. Its structure and reactivity make it a valuable tool for creating diverse molecular structures and functional groups.
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4-Nitrophenyl phosphate di(tris) salt CAS:68189-42-4
4-Nitrophenyl phosphate di(tris) salt is a chemical compound used in biochemical research and diagnostics. It is commonly utilized as a substrate for alkaline phosphatase enzyme assays. This salt, when hydrolyzed by alkaline phosphatase, produces a yellow-colored product that can be easily measured spectrophotometrically. This reaction is widely employed in various applications, including enzyme-linked immunosorbent assays (ELISAs) and phosphatase activity detection. The yellow color intensity is directly proportional to the enzyme activity, allowing for accurate quantification of alkaline phosphatase levels in biological samples. 4-Nitrophenyl phosphate di(tris) salt is stable, water-soluble, and highly sensitive, making it a popular choice for enzyme assays in biological and medical research.
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2-Methoxy-4-morpholinobenzenediazonium chloride zinc chloride double salt(21) CAS:67801-08-5
2-Methoxy-4-morpholinobenzenediazonium chloride zinc chloride double salt is a solid crystalline compound used as a reagent in organic synthesis. It consists of a diazonium cation, chloride anions, and zinc cations. This compound offers enhanced stability and solubility, making it suitable for various chemical and pharmaceutical applications.
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Guanidine Thiocyanate Sulfate CAS:593-84-0
Guanidine thiocyanate sulfate is a chemical compound derived from guanidine, thiocyanate, and sulfate ions. It is commonly used in molecular biology and biochemistry research as a chaotropic agent.
Guanidine thiocyanate sulfate is often utilized in DNA and RNA isolation protocols to disrupt cellular membranes and denature proteins, allowing for efficient extraction of nucleic acids. It helps in the solubilization of DNA and RNA, enabling their isolation and purification from various biological samples.
Due to its chaotropic properties, guanidine thiocyanate sulfate assists in breaking hydrogen bonding and other non-covalent interactions, facilitating the separation of nucleic acids from proteins, lipids, and other cellular components. It also helps in inhibiting RNase activity, ensuring the integrity and purity of the extracted nucleic acids.
