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Caveolin-1 Polyclonal Antibody
商品货号: PLA015081
适 应 性: 人,小鼠,大鼠
WB IHC IF ELISA
¥600元
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MSDS
说明书
商品描述
  • 基因名称: CAV1
  • 蛋白名称: Caveolin-1
  • Human_gene_id: 857
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=857
  • Human_swiss_prot_no: Q03135
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/Q03135/entry
  • Mouse_gene_id: 12389
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=12389
  • Mouse_swiss_prot_no: P49817
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P49817
  • Rat_swiss_prot_no: P41350
  • Rat_swiss_link: http://www.uniprot.org/uniprot/P41350
  • 特异性: Caveolin-1 Polyclonal Antibody detects endogenous levels of Caveolin-1 protein.
  • 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, IF 1:50-300, IHC 1:50-300
  • 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
  • 其他名称: CAV1; CAV; Caveolin-1
  • 实测条带: 25kD
  • 信号通路: Focal adhesion;Viral myocarditis;
  • 功能: disease:Defects in CAV1 are the cause of congenital generalized lipodystrophy type 3 (CGL3) [MIM:612526]; also called Berardinelli-Seip congenital lipodystrophy type 3 (BSCL3). Congenital generalized lipodystrophies are autosomal recessive disorders characterized by a near absence of adipose tissue, extreme insulin resistance, hypertriglyceridemia, hepatic steatosis and early onset of diabetes.,function:May act as a scaffolding protein within caveolar membranes. Interacts directly with G-protein alpha subunits and can functionally regulate their activity.,online information:Caveolin entry,PTM:The initiator methionine for isoform Beta is removed during or just after translation. The new N-terminal amino acid is then N-acetylated.,similarity:Belongs to the caveolin family.,subcellular location:Potential hairpin-like structure in the membrane. Membrane protein of caveolae.,subunit:Homooligomer. Interacts with GLIPR2, NOSTRIN, SNAP25 and syntaxin. Interacts with rotavirus A NSP4.,tissue specificity:In muscle and lung, less so in liver, brain and kidney.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Golgi apparatus membrane; Peripheral membrane protein. Cell membrane; Peripheral membrane protein. Membrane, caveola ; Peripheral membrane protein. Membrane raft . Golgi apparatus, trans-Golgi network . Colocalized with DPP4 in membrane rafts. Potential hairpin-like structure in the membrane. Membrane protein of caveolae.
  • 组织表达: Skeletal muscle, liver, stomach, lung, kidney and heart (at protein level). Expressed in the brain.
  • tag: hot
  • 科研货号: PLA015081
Caveolin-1 Polyclonal Antibody
Catalog No PLA015081
Product information
  • 基因名称: CAV1
  • 蛋白名称: Caveolin-1
  • Human_gene_id: 857
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=857
  • Human_swiss_prot_no: Q03135
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/Q03135/entry
  • Mouse_gene_id: 12389
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=12389
  • Mouse_swiss_prot_no: P49817
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P49817
  • Rat_swiss_prot_no: P41350
  • Rat_swiss_link: http://www.uniprot.org/uniprot/P41350
  • 特异性: Caveolin-1 Polyclonal Antibody detects endogenous levels of Caveolin-1 protein.
  • 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, IF 1:50-300, IHC 1:50-300
  • 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
  • 其他名称: CAV1; CAV; Caveolin-1
  • 实测条带: 25kD
  • 信号通路: Focal adhesion;Viral myocarditis;
  • 功能: disease:Defects in CAV1 are the cause of congenital generalized lipodystrophy type 3 (CGL3) [MIM:612526]; also called Berardinelli-Seip congenital lipodystrophy type 3 (BSCL3). Congenital generalized lipodystrophies are autosomal recessive disorders characterized by a near absence of adipose tissue, extreme insulin resistance, hypertriglyceridemia, hepatic steatosis and early onset of diabetes.,function:May act as a scaffolding protein within caveolar membranes. Interacts directly with G-protein alpha subunits and can functionally regulate their activity.,online information:Caveolin entry,PTM:The initiator methionine for isoform Beta is removed during or just after translation. The new N-terminal amino acid is then N-acetylated.,similarity:Belongs to the caveolin family.,subcellular location:Potential hairpin-like structure in the membrane. Membrane protein of caveolae.,subunit:Homooligomer. Interacts with GLIPR2, NOSTRIN, SNAP25 and syntaxin. Interacts with rotavirus A NSP4.,tissue specificity:In muscle and lung, less so in liver, brain and kidney.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Golgi apparatus membrane; Peripheral membrane protein. Cell membrane; Peripheral membrane protein. Membrane, caveola ; Peripheral membrane protein. Membrane raft . Golgi apparatus, trans-Golgi network . Colocalized with DPP4 in membrane rafts. Potential hairpin-like structure in the membrane. Membrane protein of caveolae.
  • 组织表达: Skeletal muscle, liver, stomach, lung, kidney and heart (at protein level). Expressed in the brain.
  • tag: hot
  • 科研货号: PLA015081
  • 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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