SLC35A2 Antibody, FITC conjugated
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中文名稱：SLC35A2兔多克隆抗體, FITC偶聯(lián)
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貨號：CSB-PA021584LC01HU
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規(guī)格：￥880
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其他：
產(chǎn)品詳情
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產(chǎn)品名稱：Rabbit anti-Homo sapiens (Human) SLC35A2 Polyclonal antibody
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Uniprot No.：
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基因名：SLC35A2
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別名：SLC35A2 antibody; UGALT antibody; UGT antibody; UGTL antibody; UDP-galactose translocator antibody; Solute carrier family 35 member A2 antibody; UDP-galactose transporter antibody; UDP-Gal-Tr antibody; UGT antibody
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宿主：Rabbit
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反應(yīng)種屬：Human
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免疫原：Recombinant Human UDP-galactose translocator protein (136-234AA)
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免疫原種屬：Homo sapiens (Human)
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標(biāo)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(chǎn)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(chǎn)品評價
相關(guān)產(chǎn)品
靶點詳情
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功能：Transports nucleotide sugars from the cytosol into Golgi vesicles where glycosyltransferases function.
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基因功能參考文獻(xiàn)：
- The short N-terminal region composed of 35 N-terminal amino-acid residues of UGT was crucial for galactosylation of N-glycans. PMID: 25451267
- UDP-galactose (SLC35A2) and UDP-N-acetylglucosamine (SLC35A3) Transporters Form Glycosylation-related Complexes with Mannoside Acetylglucosaminyltransferases (Mgats). PMID: 25944901
- De novo mutations in SLC35A2 encoding a UDP-galactose transporter cause early-onset epileptic encephalopathy. PMID: 24115232
- The data further supports the hypothesis that UGT and NGT cooperate in the UDP-Gal delivery for glycosyltransferases located in the Golgi apparatus. PMID: 23583405
- Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation. PMID: 23561849
- localization of the UDP-Gal transporter may depend on the presence of the partner splice variant PMID: 21918738
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相關(guān)疾病：Congenital disorder of glycosylation 2M (CDG2M)
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亞細(xì)胞定位：Golgi apparatus membrane; Multi-pass membrane protein.
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蛋白家族：Nucleotide-sugar transporter family, SLC35A subfamily
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數(shù)據(jù)庫鏈接：
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