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NEC1 rabbit pAb

商品貨號： PLA019904

適應(yīng) 性： 人,小鼠,大鼠

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

基因名稱： PCSK1 NEC1
蛋白名稱： 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
特異性： This antibody detects endogenous levels of NEC1 at Human/Mouse/Rat
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1：500-2000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 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.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： Cytoplasmic vesicle, secretory vesicle. Localized in the secretion granules.
科研貨號： PLA019904

NEC1 rabbit pAb

Catalog No PLA019904

Product information

基因名稱： PCSK1 NEC1
蛋白名稱： 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
特異性： This antibody detects endogenous levels of NEC1 at Human/Mouse/Rat
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1：500-2000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 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.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： Cytoplasmic vesicle, secretory vesicle. Localized in the secretion granules.
科研貨號： PLA019904

Hunan UPT Biotechnology Co.,Ltd

Website：m.tjdqdt.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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