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CYBR1 rabbit pAb
商品貨號： PLA021103
適 應(yīng) 性： 人,小鼠,大鼠
WB
￥600元
規(guī)格：
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MSDS
說明書
商品描述
  • 基因名稱： CYBRD1 DCYTB FRRS3
  • 蛋白名稱： CYBR1
  • Human_gene_id： 79901
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=79901
  • Human_swiss_prot_no： Q53TN4
  • Human_swiss_link： https://www.uniprot.org/uniprotkb/Q53TN4/entry
  • Mouse_gene_id： 73649
  • Mouse_gene_link： https://www.uniprot.org/uniprot/73649
  • Mouse_swiss_prot_no： Q925G2
  • Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q925G2
  • Rat_gene_id： 295669
  • Rat_gene_link： https://www.uniprot.org/uniprot/295669
  • Rat_swiss_prot_no： Q5RKJ2
  • Rat_swiss_link： https://www.uniprot.org/uniprotkb/Q5RKJ2
  • 特異性： This antibody detects endogenous levels of CYBR1 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： 31kD
  • 功能： cofactor:Binds 2 heme groups non-covalently.,disease:Defects in CYBRD1 may be a cause of primary hereditary hemochromatosis (HFE). HFE is an iron-loading disorder characterized by iron accumulation in parenchymal cells. Iron accumulation usually results in tissue damage and causes cirrhosis of the liver, diabetes mellitus, arthropathy, cardiomyopathy, endocrine abnormalities and an increased risk of hepatocellular carcinoma.,function:Ferric-chelate reductase that reduces Fe(3+) to Fe(2+). Present at the brush border of duodenal enterocytes where it probably reduces dietary Fe(3+) thereby facilitating its transport into the mucosal cells. Uses ascorbate as electron donor. May be involved in extracellular ascorbate recycling in erythrocyte membranes. May also act as a ferrireductase in airway epithelial cells.,induction:By iron deficiency (at protein level).,similarity:Contains 1 cytochrome b561 domain.,tissue specificity:Present in erythrocyte membranes (at protein level). Also expressed in respiratory epithelium.,
  • 相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
  • 細(xì)胞定位： Cell membrane ; Multi-pass membrane protein . Apical cell membrane ; Multi-pass membrane protein . Localized at the brush border of duodenal cells. .
  • 組織表達(dá)： Present in erythrocyte membranes (at protein level). Also expressed in respiratory epithelium.
  • 科研貨號： PLA021103
CYBR1 rabbit pAb
Catalog No PLA021103
Product information
  • 基因名稱： CYBRD1 DCYTB FRRS3
  • 蛋白名稱： CYBR1
  • Human_gene_id： 79901
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=79901
  • Human_swiss_prot_no： Q53TN4
  • Human_swiss_link： https://www.uniprot.org/uniprotkb/Q53TN4/entry
  • Mouse_gene_id： 73649
  • Mouse_gene_link： https://www.uniprot.org/uniprot/73649
  • Mouse_swiss_prot_no： Q925G2
  • Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q925G2
  • Rat_gene_id： 295669
  • Rat_gene_link： https://www.uniprot.org/uniprot/295669
  • Rat_swiss_prot_no： Q5RKJ2
  • Rat_swiss_link： https://www.uniprot.org/uniprotkb/Q5RKJ2
  • 特異性： This antibody detects endogenous levels of CYBR1 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： 31kD
  • 功能： cofactor:Binds 2 heme groups non-covalently.,disease:Defects in CYBRD1 may be a cause of primary hereditary hemochromatosis (HFE). HFE is an iron-loading disorder characterized by iron accumulation in parenchymal cells. Iron accumulation usually results in tissue damage and causes cirrhosis of the liver, diabetes mellitus, arthropathy, cardiomyopathy, endocrine abnormalities and an increased risk of hepatocellular carcinoma.,function:Ferric-chelate reductase that reduces Fe(3+) to Fe(2+). Present at the brush border of duodenal enterocytes where it probably reduces dietary Fe(3+) thereby facilitating its transport into the mucosal cells. Uses ascorbate as electron donor. May be involved in extracellular ascorbate recycling in erythrocyte membranes. May also act as a ferrireductase in airway epithelial cells.,induction:By iron deficiency (at protein level).,similarity:Contains 1 cytochrome b561 domain.,tissue specificity:Present in erythrocyte membranes (at protein level). Also expressed in respiratory epithelium.,
  • 相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
  • 細(xì)胞定位： Cell membrane ; Multi-pass membrane protein . Apical cell membrane ; Multi-pass membrane protein . Localized at the brush border of duodenal cells. .
  • 組織表達(dá)： Present in erythrocyte membranes (at protein level). Also expressed in respiratory epithelium.
  • 科研貨號： PLA021103
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