2-(2-Methyl-1-piperidinyl)isonicotinic+acid
Catalog Number:
(10428-642)
Supplier:
Bioss
Description:
In embryonic stem (ES) cells, plays a crucial role in the differentiation potential, particularly along the neural lineage, regulating gene induction and H3 'Lys-4' methylation at key developmental loci, including that mediated by retinoic acid (By similarity). As part of the MLL1/MLL complex, involved in mono-, di- and trimethylation at 'Lys-4' of histone H3. Histone H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation.
Catalog Number:
(EM8.18367.0001)
Supplier:
Spectrum Chemicals
Description:
Dimethylamine Hydrochloride, purity: 98 %, CAS number: 506-59-2, Molecular Formula: C2H7N.HCl, Molecular weight: 81.55, Form: Solid, synonyms: Hydrochloric acid dimethylamine, Methanamine, N-methyl-, hydrochloride, Dimethylammonium chloride, size: 500 g
Supplier:
Thermo Scientific Chemicals
Description:
Packaged under argon in resealable ChemSeal bottle
Supplier:
AMBEED, INC
Description:
1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)pyrrolidine, Purity: 97%, CAS number: 884507-39-5, Appearance: White to Yellow Solid, Storage: Inert atmosphere, Room Temperature, Size: 1G
Catalog Number:
(103008-180)
Supplier:
Anaspec Inc
Description:
This peptide is derived from Histone H3 21-44 amino acids, and is usually used as a substrate for methylation assays. It has been used as a substrate for protein arginine methyltransferases
Sequence:ATKAARKSAPATGGVKKPHRYRPG MW:2505.9 Da % peak area by HPLC:95 Storage condition:-20° C
Catalog Number:
(77975-923)
Supplier:
LGC STANDARDS
Description:
Type PSU1400, Viscosity Reference Standard, Paragon Scientific, LGC Standards
Catalog Number:
(10406-526)
Supplier:
Bioss
Description:
This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
Supplier:
Spectrum Chemicals
Description:
Propylene Carbonate, Reagent, is an organic compound that is a liquid that is both colorless and odorless. Used in a range of applications, the most notable one is as a polar and aprotic solvent in syntheses. It is also used as a high-permittivity component as it has a dielectric constant of 64. Its reagent grade means this is the highest quality commercially available for this chemical and that the American Chemical Society has not officially set any specifications for this material.
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Supplier:
Electron Microscopy Sciences
Description:
A non-carcinogenic substitute for Propylene Oxide, used in tissueprocessing for TEM. Good for infiltration with EMbed-812 or other Epon-812 substitutes. Tarnowski, sB.I. et al, EMSA proceedings, Detroit, MI page 38 (1984).
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Catalog Number:
(77976-099)
Supplier:
LGC STANDARDS
Description:
Norbuprenorphine-D3, 0.1mg/ml in Methanol, Lipomed, LGC Standards
Supplier:
Spectrum Chemicals
Description:
Erioglaucine, also known as Brilliant Blue FCF, is commonly a colorant for foods like ice cream, processed peas, and dairy products. Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use. These materials may or may not have a Certificate of Analysis available.
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Supplier:
BeanTown Chemical
Description:
CAS: 102195-80-2; MDL No: MFCD01861778
Powder; Molecular Formula: C11H17NO5; MW: 243.26
Melting Point: 42-46°; Flash point: <gt/>110°C (<gt/>230°F)
Optical Rotation: [α]22/D +14.0°, c = 1 in chloroform
Air Sensitive, Heat Sensitive, Moisture Sensitive
Catalog Number:
(10671-736)
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.
Catalog Number:
(10671-756)
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.
Catalog Number:
(10406-524)
Supplier:
Bioss
Description:
This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009].
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