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Potassium+tri(1H-imidazol-1-yl)hydroborate


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Supplier:  MP Biomedicals
Description:   Quinhydrone is addition compound of one mol hydroquinone and one mol Benzoquinone.
Quinhydrone electrode is a type of redox electrode which can be used to measure the hydrogen ion concentration (pH) of a solution in a chemical experiment.
Quinhydrone/methanol treatment for the measurement of carrier lifetime in crystalline silicon substrates has been reported. Surface passivation of silicon substrates by quinhydrone/ethanol treatment has been investigated.
Room Temperature
Supplier:  Bioss
Description:   Repair polymerase that plays a key role in base-excision repair. Has 5'-deoxyribose-5-phosphate lyase (dRP lyase) activity that removes the 5' sugar phosphate and also acts as a DNA polymerase that adds one nucleotide to the 3' end of the arising single-nucleotide gap. Conducts 'gap-filling' DNA synthesis in a stepwise distributive fashion rather than in a processive fashion as for other DNA polymerases.
Supplier:  Bioss
Description:   Insulin decreases blood glucose concentration. It increases cell permeability to monosaccharides, amino acids and fatty acids. It accelerates glycolysis, the pentose phosphate cycle, and glycogen synthesis in liver.
Catalog Number: (RL009-0634)

Supplier:  Rockland Immunochemical
Description:   1mg. Antibody Concentration: 1 mg/mL. Biotin/Protein: 10-20 BAC molecules per Human Transferrin molecule. Buffer: 0.02M potassium phosphate, 0.15M sodium chloride, pH 7.2. Stabilizer: 10 mg/mL BSA IgG and protease free. For research. Lyophilized.
Small Business Enterprise Minority or Woman-Owned Business Enterprise
Supplier:  MOLTOX Molecular Toxicology
Supplier:  Matrix Scientific
Description:   ((2R, 3S, 4R, 5R)-5-(4-Amino-2-Oxopyrimidin-1(2H)-Yl)-3, 4-Dihydroxytetrahydrofuran-2-Yl)Methyl Dihydrogen Phosphate, purity: 95+%, CAS number: 63-37-6, Molecular formula: C9H14N3O8P, Molecular weight: 323.2, Size: 100G
Supplier:  IBI Scientific
Description:   IBI Cell Culture Grade, Pyrogen/Endotoxin Free Water is prepared for nuclear transfer, transfection, transformation, cell and tissue culture, LAL testing, and all other aqueous solution preparations that require stringent quality control.
Supplier:  Bioss
Description:   The inositol polyphosphate 5-phosphatases selectively remove the phosphate from the 5-position of various phosphatidylinositols, which generate second messengers in response to extracellular signals. Synaptojanins are characterized by an N-terminal SAC1-like sequence, a central 5-phosphate domain, and a unique C-terminal sequence and have been shown to use phosphatidylinositol 4,5-bisphosphate as a substrate. Synaptojanins exist as two isoforms, synaptojanin 1 and 2, which differ in the C-terminal domain, and each isoform has multiple variants produced by alternative splicing. Synaptojanin 1 is expressed as two major forms: the shorter is found in brain while the longer is expressed in peripheral tissues. Eight splice variants of synaptojanin 2 have been detected, including a brain specific isoform. Synaptojanins are thought to participate in the endocytosis of synaptic vesicles and the regulation of the actin cytoskeleton.
Catalog Number: (10748-570)

Supplier:  Prosci
Description:   GAPDH Antibody: Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) catalyzes the reversible oxidative phosphorylation of glyceraldehyde-3-phosphate in the presence of inorganic phosphate and nicotinamide adenine dinucleotide (NAD), an important energy-yielding step in carbohydrate metabolism. Recent evidence suggests that it also is involved in a number of cellular processes such as membrane fusion, phosphotransferase activity, DNA replication and repair, and nuclear RNA export. GAPDH has also been implicated in playing a role in different pathologies such as cancer progression, apoptosis, and neuronal diseases such as Alzheimer's and Huntington's disease. GAPDH is constitutively expressed at high levels in almost all tissues and cell lines making it ideal for use as a loading control marker in immunoblots.
Supplier:  Bioss
Description:   Members of the class-III pyridoxal-phosphate-dependent aminotransferase family, such as AGXT2, catalyze the conversion of glyoxylate to glycine using L-alanine as the amino donor. AGXT2 protects from asymmetric dimethylarginine (ADMA)-induced inhibition in nitric oxide (NO) production. Elevated blood concentrations of ADMA, a methyl derivate of the amino acid arginine and an endogenous inhibitor of nitric oxide (NO) synthase, is produced by the physiological degradation of methylated proteins and is found in association with diabetes, hypertension, congestive heart failure and atherosclerosis. AGXT2L2 (alanine-glyoxylate aminotransferase 2-like 2) is a 450 amino acid pyridoxal phosphate that exists as a homotetramer. Belonging to the class-III pyridoxal-phosphate-dependent aminotransferase family, AGXT2L2 localizes to the mitochondria and exists as three alternatively spliced isoforms. Encoded by a gene located on human chromosome 5q35.3, AGXT2L2 may have similar functions as AGXT2.
Supplier:  TCI America
Description:   CAS Number: 165534-43-0
Molecular Formula: C11H14N3O5P
Molecular Weight: 299.22
Purity/Analysis Method: >98.0% (HPLC,N)
Form: Crystal
Melting point (°C): 73
MSDS SDS

Supplier:  Bioss
Description:   Required for the transport of mannose 6-phosphate receptors (MPR) from endosomes to the trans-Golgi network.
Catalog Number: (76666-952)

Supplier:  AMBEED, INC
Description:   4-Propylphenol, Purity: 98%, CAS Number: 645-56-7, Appearance: Yellow to Dark red to Dark Brown Liquid or Solid or Semi-solid or lump, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 25G
Supplier:  G-Biosciences
Description:   (0.1M Sodium phosphate, 0.15M NaCl, pH 7.5), 100ml
Catalog Number: (TS46183-0010)

Supplier:  THERMO FISHER SCIENTIFIC CHEMICALS
Description:   Miltefosine 98%
Catalog Number: (10110-006)

Supplier:  Prosci
Description:   ALDOA is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia.This gene product, Aldolase A (fructose-bisphosphate aldolase) is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing of this gene results in multiple transcript variants which encode the same protein.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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