首页 > 抗体 > 一抗 > 其它 > SGLT-1 Polyclonal Antibody
SGLT-1 Polyclonal Antibody
商品货号: PLA018097
适 应 性: 人,小鼠,大鼠
WB IHC ELISA
¥600元
规格:
在线咨询
MSDS
说明书
商品描述
  • 基因名称: SLC5A1
  • 蛋白名称: Sodium/glucose cotransporter 1
  • Human_gene_id: 6523
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6523
  • Human_swiss_prot_no: P13866
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P13866/entry
  • Mouse_gene_id: 20537
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20537
  • Mouse_swiss_prot_no: Q8C3K6
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/Q8C3K6
  • Rat_gene_id: 25552
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=25552
  • Rat_swiss_prot_no: P53790
  • Rat_swiss_link: http://www.uniprot.org/uniprot/P53790
  • 特异性: SGLT-1 Polyclonal Antibody detects endogenous levels of SGLT-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;IHC-p 1:50-300; ELISA 2000-20000
  • 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: SLC5A1; NAGT; SGLT1; Sodium/glucose cotransporter 1; Na(+)/glucose cotransporter 1; High affinity sodium-glucose cotransporter; Solute carrier family 5 member 1
  • 实测条带: 75kD
  • 功能: disease:Defects in SLC5A1 are the cause of congenital glucose/galactose malabsorption (GGM) [MIM:606824]. GGM is an intestinal monosaccharide transporter deficiency. It is an autosomal recessive disorder manifesting itself within the first weeks of life. It is characterized by severe diarrhea and dehydration which are usually fatal unless glucose and galactose are eliminated from the diet.,function:Actively transports glucose into cells by Na(+) cotransport with a Na(+) to glucose coupling ratio of 2:1. Efficient substrate transport in mammalian kidney is provided by the concerted action of a low affinity high capacity and a high affinity low capacity Na(+)/glucose cotransporter arranged in series along kidney proximal tubules.,PTM:N-glycosylation is not necessary for the cotransporter function.,similarity:Belongs to the sodium:solute symporter (SSF) (TC 2.A.21) family.,tissue specificity:Expressed mainly in intestine and kidney.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Apical cell membrane ; Multi-pass membrane protein .
  • 组织表达: Expressed in intestine (PubMed:2490366). Expressed in endometrial cells (PubMed:28974690).
  • tag: hot
  • 科研货号: PLA018097
SGLT-1 Polyclonal Antibody
Catalog No PLA018097
Product information
  • 基因名称: SLC5A1
  • 蛋白名称: Sodium/glucose cotransporter 1
  • Human_gene_id: 6523
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6523
  • Human_swiss_prot_no: P13866
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P13866/entry
  • Mouse_gene_id: 20537
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20537
  • Mouse_swiss_prot_no: Q8C3K6
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/Q8C3K6
  • Rat_gene_id: 25552
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=25552
  • Rat_swiss_prot_no: P53790
  • Rat_swiss_link: http://www.uniprot.org/uniprot/P53790
  • 特异性: SGLT-1 Polyclonal Antibody detects endogenous levels of SGLT-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;IHC-p 1:50-300; ELISA 2000-20000
  • 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: SLC5A1; NAGT; SGLT1; Sodium/glucose cotransporter 1; Na(+)/glucose cotransporter 1; High affinity sodium-glucose cotransporter; Solute carrier family 5 member 1
  • 实测条带: 75kD
  • 功能: disease:Defects in SLC5A1 are the cause of congenital glucose/galactose malabsorption (GGM) [MIM:606824]. GGM is an intestinal monosaccharide transporter deficiency. It is an autosomal recessive disorder manifesting itself within the first weeks of life. It is characterized by severe diarrhea and dehydration which are usually fatal unless glucose and galactose are eliminated from the diet.,function:Actively transports glucose into cells by Na(+) cotransport with a Na(+) to glucose coupling ratio of 2:1. Efficient substrate transport in mammalian kidney is provided by the concerted action of a low affinity high capacity and a high affinity low capacity Na(+)/glucose cotransporter arranged in series along kidney proximal tubules.,PTM:N-glycosylation is not necessary for the cotransporter function.,similarity:Belongs to the sodium:solute symporter (SSF) (TC 2.A.21) family.,tissue specificity:Expressed mainly in intestine and kidney.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Apical cell membrane ; Multi-pass membrane protein .
  • 组织表达: Expressed in intestine (PubMed:2490366). Expressed in endometrial cells (PubMed:28974690).
  • tag: hot
  • 科研货号: PLA018097
  • 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.
普拉特泽实验室电话助手

4006916686

扫码咨询