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  4. Biochemical Assay Reagents

Biochemical Assay Reagents

Biochemical agents refers to the life science research related to biological material or organic compounds. Due to a wide range of life sciences, rapid development, and therefore a wide variety of such agents, complex in nature. There are electrophoresis reagents, chromatography reagents, centrifuged reagents, immunological reagent, labeled reagent, staining agents, penetration agents and carcinogens variable, insecticides, culture, buffering agents, electron microscopy reagents, protein and nucleic acid precipitating agent, condensing agent ultrafiltration membrane, clinical diagnostic reagents, dyes, antioxidants, preservatives, detergents and surfactants, standard biochemical reagents, biochemical reagents quality control materials, separation material, etc..

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-W008321
    6-Bromo-3,4-dihydro-1(2H)-naphthalenone
    		99.47%
    6-Bromo-3,4-dihydro-1 (2H)-naphthalenone is a synthetic intermediate. 6-Bromo-3,4-dihydro-1 (2H)-naphthalenone can be used for the synthesis of 2-Benzyl-6-bromo-3,4-dihydro-1 (2H)-naphthalenone. 6-Bromo-3,4-dihydro-1 (2H)-naphthalenone can be applied to the development of hypoglycemic agents.
    6-Bromo-3,4-dihydro-1(2H)-naphthalenone
  • HY-69094
    6-Bromoquinoxaline
    		99.87%
    6-Bromoquinoxaline is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    6-Bromoquinoxaline
  • HY-126164
    LK 614
    		99.76%
    LK 614 is a membrane permeable iron chelator that can be used to study the protective effects against L-Histidine (HY-N0832)-induced cell damage.
    LK 614
  • HY-W507393
    Dipropylenetriamine NONOate
    		98%
    Dipropylenetriamine NONOate (DPTA-NO) is a NO donor, which spontaneously dissociates in a pH-dependent, first-order process with a half-life of three hours and five hours at 37°C and 22-25°C, pH 7.4, respectively.
    Dipropylenetriamine NONOate
  • HY-W005864
    3-Hydroxyphenylboronic acid pinacol ester
    		≥98.0%
    3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    3-Hydroxyphenylboronic acid pinacol ester
  • HY-W127534
    Tricaproin
    		99.90%
    TricaproinIt is an organic compound belonging to the class of triacylglycerols. It consists of three molecules of caproic acid esterified to the glycerin backbone, with a mild fatty smell. TricaproinIt has a variety of applications in the cosmetic and personal care industries, especially as an emollient and conditioning agent in skin and hair care products. Additionally, it is used as a lubricant and surfactant in industrial settings.
    Tricaproin
  • HY-W005012
    1,3-Dibromo-2,2-dimethoxypropane
    		99.98%
    1,3-Dibromo-2,2-dimethoxypropane is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    1,3-Dibromo-2,2-dimethoxypropane
  • HY-P2495A
    OVA (241-270) TFA
    		99.36%
    OVA (241-270) TFA, a non-specific cytotoxic T lymphocyte (CTL) peptide, is a fragmented peptide of OVA (ovalbumin) antigen.
    OVA (241-270) TFA
  • HY-Y0030A
    3-Hydroxypicolinic acid, matrix substance for MALDI-MS
    		99.15%
    3-Hydroxypicolinic acid, matrix substance for MALDI-MS is a matrix. 3-Hydroxypicolinic acid, matrix substance for MALDI-MS coordinates with metal ions such as copper to form complexes with cytotoxic and antimycobacterial activity. 3-Hydroxypicolinic acid, matrix substance for MALDI-MS is used for the analysis of oligodeoxynucleotides in matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS). 3-Hydroxypicolinic acid, matrix substance for MALDI-MS is useful for nucleic acid analysis and anti-tuberculosis compound development.
    3-Hydroxypicolinic acid, matrix substance for MALDI-MS
  • HY-P3263
    Glutamate oxidase
    Glutamate oxidase (L-Glutamate oxidase) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Glutamate oxidase is expressed in E. Coli. Glutamate oxidase can be used to produce α-ketoglutaric acid from l-glutamic acid.
    Glutamate oxidase
  • HY-W010407
    Cyanuric acid
    		98.69%
    1,3,5-Triazine-2,4,6-triol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    Cyanuric acid
  • HY-D1056F
    Biotin-Lipopolysaccharide, from E.coli O111:B4
    Biotin-Lipopolysaccharide, from E.coli O111:B4 (Biotin-LPS, from Escherichia coli (O111:B4)) is a biotin-conjugated Lipopolysaccharide (LPS) (HY-D1056A1) that can be coupled with streptavidin protein. Biotin-Lipopolysaccharide, from E.coli O111:B4 can be used to identify Lipopolysaccharide ligands. Lipopolysaccharides, from E. coli O111:B4 (LPS, from Escherichia coli (O111:B4)) are endotoxins and TLR4 activators extracted from Escherichia coli (E. coli O111:B4) and are classified as S (smooth) type LPS. Lipopolysaccharides, from E. coli O111:B4 possess the typical three-part structure: O-antigen, R3-type core oligosaccharide, and lipid A. Lipopolysaccharides, from E. coli O111:B4 activate TLR-4 in immune cells and can cause significant gastric diseases. Lipopolysaccharides, from E. coli O111:B4 can also induce M1-type polarization in mouse macrophages.
    It is recommended to prepare a solution with concentration ≥2 mg/mL. Vortex thoroughly for more than 10 minutes. Due to the adsorption characteristics of LPS, silanized container or low adsorption centrifuge tubes should be used for aliquoting and storage, and mix thoroughly before use.
    Biotin-Lipopolysaccharide, from E.coli O111:B4
  • HY-W003050
    2-Isopropylbenzeneboronic acid
    		99.94%
    2-Isopropylbenzeneboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    2-Isopropylbenzeneboronic acid
  • HY-D1005A25
    Poloxamer 403 (P123)
    Poloxamer 403 P123 is a block copolymer of polyoxyethylene and polyoxypropylene with an average molecular weight of 5750. Poloxamer has the ability to inhibit P-gp. Poloxamer 403 increases creatine kinase levels. Poloxamer 403 is myotoxic.
    Poloxamer 403 (P123)
  • HY-W009020
    β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate
    β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
    β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate
  • HY-160291
    Trivalent GalNAc-DBCO
    Trivalent GalNAc-DBCO can be used for oligonucleotide coupling.
    Trivalent GalNAc-DBCO
  • HY-W004116
    2-Benzofurylboronic acid
    		99.95%
    Benzofuran-2-boronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    2-Benzofurylboronic acid
  • HY-W017032
    1H-Pyrazole-1-carboximidamide hydrochloride
    		99.86%
    1H-Pyrazole-1-carboximidamide hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    1H-Pyrazole-1-carboximidamide hydrochloride
  • HY-Y0395
    3-Carboxyphenylboronic acid
    		99.97%
    3-Carboxyphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    3-Carboxyphenylboronic acid
  • HY-W088001
    Bromophenol blue sodium
    Bromophenol blue sodium salt is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    Bromophenol blue sodium
Cat. No. Product Name / Synonyms Application Reactivity