You Searched For: 2,3-Dimethylphenylboronic+acid


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Supplier: TCI America
Description: CAS Number: 27214-00-2
MDL Number: MFCD00042643
Molecular Formula: C3H9O6P
Molecular Weight: 210.13
Purity/Analysis Method: >95.0% (T)
Form: Crystal

SDS

Catalog Number: (76110-740)
Supplier: Bioss
Description: BPGM (2,3-bisphosphoglycerate mutase) is a 259 amino acid protein that belongs to the phosphoglycerate mutase family and exists as a homodimer that plays a crucial role in the regulation of hemoglobin oxygen. Specifically, BPGM catalyzes the conversion of 3-D-glyceroyl phosphate to 2,3-bisD-glycerate (2,3-BPG), a reaction that is essential for controlling the concentration of 2,3-BPG within the cell. The gene encoding BPGM maps to human chromosome 7, which houses over 1000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Involvement in disease: Defects in BPGM are the cause of bisphosphoglycerate mutase deficiency (BPGMD). A disease characterized by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.


Catalog Number: (10495-590)
Supplier: Bioss
Description: BPGM (2,3-bisphosphoglycerate mutase) is a 259 amino acid protein that belongs to the phosphoglycerate mutase family and exists as a homodimer that plays a crucial role in the regulation of hemoglobin oxygen. Specifically, BPGM catalyzes the conversion of 3-D-glyceroyl phosphate to 2,3-bisD-glycerate (2,3-BPG), a reaction that is essential for controlling the concentration of 2,3-BPG within the cell. The gene encoding BPGM maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Involvement in disease:Defects in BPGM are the cause of bisphosphoglycerate mutase deficiency (BPGMD) . A disease characterized by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.


Supplier: TCI America
Description: CAS Number: 1149-23-1
MDL Number: MFCD00005951
Molecular Formula: C13H19NO4
Molecular Weight: 253.30
Purity/Analysis Method: >98.0% (HPLC,N)
Form: Crystal
Melting point (°C): 183
Lambda max.: 374 nm (EtOH)
Catalog Number: (89515-566)
Supplier: Abgent
Description: polyclonal antibody Isotype: Rabbit Ig, Species Reactivity: human, Target/specificity: This PLGLA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 23-48 amino acids from the N-terminal region of human PLGLA.


Catalog Number: (76110-738)
Supplier: Bioss
Description: BPGM (2,3-bisphosphoglycerate mutase) is a 259 amino acid protein that belongs to the phosphoglycerate mutase family and exists as a homodimer that plays a crucial role in the regulation of hemoglobin oxygen. Specifically, BPGM catalyzes the conversion of 3-D-glyceroyl phosphate to 2,3-bisD-glycerate (2,3-BPG), a reaction that is essential for controlling the concentration of 2,3-BPG within the cell. The gene encoding BPGM maps to human chromosome 7, which houses over 1000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Involvement in disease: Defects in BPGM are the cause of bisphosphoglycerate mutase deficiency (BPGMD). A disease characterized by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.


Supplier: MilliporeSigma
Description: Ultrapure grade, Causes severe skin burns and eye damage, Synonym Hydrogen chloride solution.
Supplier: Bachem Americas
Description: Sequence: Fmoc-Homocys(Trt)-OH

Catalog Number: (10082-464)
Supplier: Proteintech
Description: ACSM2A(Acyl-coenzyme A synthetase ACSM2A, mitochondrial) is also named as ACSM2, MACS2 and belongs to the ATP-dependent AMP-binding enzyme family. It acts as a medium-chain fatty acid : CoA ligase with the caculated molecular weight of 64 kDa and acts on acids from C(4) to C(11) and on the corresponding 3-hydroxy- and 2,3- or 3,4-unsaturated acids.


Supplier: Wards
Description: These lightweight and durable polypropylene stoppers are acid proof and autoclavable.

Catalog Number: (10110-250)
Supplier: Prosci
Description: ST6GALNAC4 is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. ST6GALNAC4 prefers glycoproteins rather than glycolipids as substrates and shows restricted substrate specificity, utilizing only the trisaccharide sequence Neu5Ac-alpha-2,3-Gal-beta-1,3-GalNAc. In addition, it is involved in the synthesis of ganglioside GD1A from GM1B. ST6GALNAC4 is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. It is a member of glycosyltransferase family 29.The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein prefers glycoproteins rather than glycolipids as substrates and shows restricted substrate specificity, utilizing only the trisaccharide sequence Neu5Ac-alpha-2,3-Gal-beta-1,3-GalNAc. In addition, it is involved in the synthesis of ganglioside GD1A from GM1B. The encoded protein is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. This protein is a member of glycosyltransferase family 29. Transcript variants encoding different isoforms have been found for this gene.


Supplier: Thermo Scientific Chemicals
Description: Catalyzes the regio selective ring opening of 2,3 epoxy alcohols and acids
Supplier: Thermo Scientific Chemicals
Description: (-)-Di-p-toluoyl-L-tartaric acid 98%
Catalog Number: (CAPI24308)
Supplier: Thermo Scientific
Description: Pierce™ Hydrochloric acid solution, sequencing grade, is purified and packaged to ensure a ninhydrin-negative blank on hydrolysis

Catalog Number: (89521-266)
Supplier: Abgent
Description: polyclonal antibody, Isotype: Rabbit Ig , Species reactivity: Human, Gene ID: 632, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 23-52 amino acids from the Central region of human BGLAP


Catalog Number: (89518-188)
Supplier: Abgent
Description: Polyclonal antibody, Isotype: Rabbit Ig, Species Reactivity: Human , Gene ID: 124975 , Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 23-49 amino acids from the N-terminal region of human GGT6


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