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PYGM rabbit pAb
商品货号: PLA009989
适 应 性: 人,小鼠,大鼠
WB
¥600元
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MSDS
说明书
商品描述
  • 发货日期: 7
  • 基因名称: PYGM
  • 蛋白名称: PYGM
  • Human_gene_id: 5837
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5837
  • Human_swiss_prot_no: P11217
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P11217/entry
  • Mouse_gene_id: 19309
  • Mouse_gene_link: https://www.uniprot.org/uniprot/19309
  • Mouse_swiss_prot_no: Q9WUB3
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q9WUB3
  • Rat_swiss_prot_no: P09812
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/P09812
  • 特异性: This antibody detects endogenous levels of PYGM at Human/Mouse/Rat
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 93kD
  • 功能: catalytic activity:(1,4-alpha-D-glucosyl)(n) + phosphate = (1,4-alpha-D-glucosyl)(n-1) + alpha-D-glucose 1-phosphate.,cofactor:Pyridoxal phosphate.,disease:Defects in PYGM are the cause of glycogen storage disease type 5 (GSD5) [MIM:232600]; also known as McArdle disease. GSD5 is a metabolic disorder resulting in myopathy characterized by exercise intolerance, cramps, muscle weakness and recurrent myoglobinuria.,enzyme regulation:Activity of phosphorylase is controlled both by allosteric means (through the noncovalent binding of metabolites) and by covalent modification. Thus AMP allosterically activates, whereas ATP, ADP, and glucose-6-phosphate allosterically inhibit, phosphorylase B.,function:Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties.,PTM:Phosphorylation of Ser-15 converts phosphorylase B (unphosphorylated) to phosphorylase A.,similarity:Belongs to the glycogen phosphorylase family.,subunit:Homodimer. Dimers associate into a tetramer to form the enzymatically active phosphorylase A.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: cytoplasm,cytosol,extracellular exosome,
  • 科研货号: PLA009989
PYGM rabbit pAb
Catalog No PLA009989
Product information
  • 发货日期: 7
  • 基因名称: PYGM
  • 蛋白名称: PYGM
  • Human_gene_id: 5837
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5837
  • Human_swiss_prot_no: P11217
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P11217/entry
  • Mouse_gene_id: 19309
  • Mouse_gene_link: https://www.uniprot.org/uniprot/19309
  • Mouse_swiss_prot_no: Q9WUB3
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q9WUB3
  • Rat_swiss_prot_no: P09812
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/P09812
  • 特异性: This antibody detects endogenous levels of PYGM at Human/Mouse/Rat
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 93kD
  • 功能: catalytic activity:(1,4-alpha-D-glucosyl)(n) + phosphate = (1,4-alpha-D-glucosyl)(n-1) + alpha-D-glucose 1-phosphate.,cofactor:Pyridoxal phosphate.,disease:Defects in PYGM are the cause of glycogen storage disease type 5 (GSD5) [MIM:232600]; also known as McArdle disease. GSD5 is a metabolic disorder resulting in myopathy characterized by exercise intolerance, cramps, muscle weakness and recurrent myoglobinuria.,enzyme regulation:Activity of phosphorylase is controlled both by allosteric means (through the noncovalent binding of metabolites) and by covalent modification. Thus AMP allosterically activates, whereas ATP, ADP, and glucose-6-phosphate allosterically inhibit, phosphorylase B.,function:Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties.,PTM:Phosphorylation of Ser-15 converts phosphorylase B (unphosphorylated) to phosphorylase A.,similarity:Belongs to the glycogen phosphorylase family.,subunit:Homodimer. Dimers associate into a tetramer to form the enzymatically active phosphorylase A.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: cytoplasm,cytosol,extracellular exosome,
  • 科研货号: PLA009989
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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