SLC52A1 Antibody, FITC conjugated
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中文名稱：SLC52A1兔多克隆抗體, FITC偶聯
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貨號：CSB-PA878904LC01HU
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規格：￥880
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) SLC52A1 Polyclonal antibody
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Uniprot No.：
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基因名：SLC52A1
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別名：FLJ10060 antibody; G protein coupled receptor 172B antibody; GPCR antibody; GPCR42 antibody; hRFT1 antibody; member 1 antibody; OTTHUMP00000125300 antibody; PAR2 antibody; PERV-A receptor 2 antibody; PERVA receptor 2 antibody; Porcine endogenous retrovirus A receptor 2 antibody; Protein GPR172B antibody; Putative G protein coupled receptor GPCR42 antibody; Riboflavin transporter 1 antibody; riboflavin transporter antibody; S52A1_HUMAN antibody; SLC52A1 antibody; Solute carrier family 52 antibody; Solute carrier family 52, riboflavin transporter, member 1 antibody
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宿主：Rabbit
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反應種屬：Human
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免疫原：Recombinant Human Solute carrier family 52, riboflavin transporter, member 1 protein (212-279AA)
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免疫原種屬：Homo sapiens (Human)
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標記方式：FITC
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克隆類型：Polyclonal
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抗體亞型：IgG
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純化方式：>95%, Protein G purified
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濃度：It differs from different batches. Please contact us to confirm it.
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保存緩沖液：Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 -
產品提供形式：Liquid
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儲存條件：Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期：Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途：For Research Use Only. Not for use in diagnostic or therapeutic procedures.
產品評價
相關產品
靶點詳情
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功能：Plasma membrane transporter mediating the uptake by cells of the water soluble vitamin B2/riboflavin that plays a key role in biochemical oxidation-reduction reactions of the carbohydrate, lipid, and amino acid metabolism. Humans are unable to synthesize vitamin B2/riboflavin and must obtain it via intestinal absorption.; (Microbial infection) May function as a cell receptor to retroviral envelopes similar to the porcine endogenous retrovirus (PERV-A).
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基因功能參考文獻：
- We here report a case of transient MADD, caused by a heterozygous intronic variation, c.1134+11G>A, in the SLC52A1 gene encoding RFVT1. This variation creates a binding site for the splice inhibitory hnRNP A1 protein and causes exon 4 skipping. Riboflavin deficiency and maternal malnutrition during pregnancy might have been the determining factor in the outcome of this case. PMID: 29122468
- In HT-29 cells, the RFVT1 protein level was drastically lower. In tumor tissues of patients with CRC, RFVT1 content was reduced at both protein and mRNA levels compared to normal mucosa. PMID: 29715086
- results are the first to reveal the identity of the minimal SLC52A1 promoter and to establish an important role for Sp-1 in its activity PMID: 25284511
- data suggest that MMND is a distinct clinical subgroup of childhood onset MND patients where the known genetic defects are so far negative. PMID: 24139842
- summary of recent findings on the cloning, nomenclature, functional characterization and genetic diseases of RFVT1/SLC52A1, RFVT2/SLC52A2 and RFVT3/SLC52A3 [review] PMID: 23506902
- Intestinal riboflavin uptake process undergoes differentiation-dependent upregulation and suggest that this is mediated (at least in part) via transcriptional mechanisms of SLC52A1 and SLC52A3. PMID: 23413253
- We demonstrated that TFAP-2gamma is one of the transcription factors involved in the PAR-2 expression in human villous trophoblast cells. PMID: 22702469
- Identification/characterization riboflavin trasporter (RFT1) as a novel riboflavin transporter. PMID: 18632736
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相關疾病：Riboflavin deficiency (RBFVD)
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亞細胞定位：Cell membrane; Multi-pass membrane protein.
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蛋白家族：Riboflavin transporter family
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組織特異性：Widely expressed. Highly expressed in the testis, placenta and small intestine. Expressed at lower level in other tissues.
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數據庫鏈接：
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