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NEC1 rabbit pAb
商品货号: PLA019904
适 应 性: 人,小鼠,大鼠
WB
¥600元
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MSDS
说明书
商品描述
  • 基因名称: PCSK1 NEC1
  • 蛋白名称: NEC1
  • Human_gene_id: 5122
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5122
  • Human_swiss_prot_no: P29120
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P29120/entry
  • Mouse_gene_id: 18548
  • Mouse_gene_link: https://www.uniprot.org/uniprot/18548
  • Mouse_swiss_prot_no: P63239
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P63239
  • Rat_gene_id: 100911216
  • Rat_gene_link: https://www.uniprot.org/uniprot/100911216
  • Rat_swiss_prot_no: P28840
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/P28840
  • 特异性: This antibody detects endogenous levels of NEC1 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: 83kD
  • 功能: catalytic activity:Release of protein hormones, neuropeptides and renin from their precursors, generally by hydrolysis of -Lys-Arg-|- bonds.,cofactor:Calcium.,disease:Defects in PCSK1 are the cause of proprotein convertase 1 deficiency (PC1 deficiency) [MIM:600955]. PC1 deficiency is characterized by obesity, hypogonadism, hypoadrenalism, reactive hypoglycemia as well as marked small-intestinal absorptive dysfunction It is due to impaired processing of prohormones.,function:Involved in the processing of hormone and other protein precursors at sites comprised of pairs of basic amino acid residues. Substrates include POMC, renin, enkephalin, dynorphin, somatostatin and insulin.,polymorphism:Genetic variations in PCSK1 define the body mass index quantitative trait locus 12 (BMIQ12) [MIM:612362]. Variance in body mass index is a susceptibility factor for obesity.,similarity:Belongs to the peptidase S8 family.,similarity:Belongs to the peptidase S8 family. Furin subfamily.,subcellular location:Localized in the secretion granules.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cytoplasmic vesicle, secretory vesicle. Localized in the secretion granules.
  • 科研货号: PLA019904
NEC1 rabbit pAb
Catalog No PLA019904
Product information
  • 基因名称: PCSK1 NEC1
  • 蛋白名称: NEC1
  • Human_gene_id: 5122
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5122
  • Human_swiss_prot_no: P29120
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P29120/entry
  • Mouse_gene_id: 18548
  • Mouse_gene_link: https://www.uniprot.org/uniprot/18548
  • Mouse_swiss_prot_no: P63239
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P63239
  • Rat_gene_id: 100911216
  • Rat_gene_link: https://www.uniprot.org/uniprot/100911216
  • Rat_swiss_prot_no: P28840
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/P28840
  • 特异性: This antibody detects endogenous levels of NEC1 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: 83kD
  • 功能: catalytic activity:Release of protein hormones, neuropeptides and renin from their precursors, generally by hydrolysis of -Lys-Arg-|- bonds.,cofactor:Calcium.,disease:Defects in PCSK1 are the cause of proprotein convertase 1 deficiency (PC1 deficiency) [MIM:600955]. PC1 deficiency is characterized by obesity, hypogonadism, hypoadrenalism, reactive hypoglycemia as well as marked small-intestinal absorptive dysfunction It is due to impaired processing of prohormones.,function:Involved in the processing of hormone and other protein precursors at sites comprised of pairs of basic amino acid residues. Substrates include POMC, renin, enkephalin, dynorphin, somatostatin and insulin.,polymorphism:Genetic variations in PCSK1 define the body mass index quantitative trait locus 12 (BMIQ12) [MIM:612362]. Variance in body mass index is a susceptibility factor for obesity.,similarity:Belongs to the peptidase S8 family.,similarity:Belongs to the peptidase S8 family. Furin subfamily.,subcellular location:Localized in the secretion granules.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cytoplasmic vesicle, secretory vesicle. Localized in the secretion granules.
  • 科研货号: PLA019904
  • 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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