SLC35A2 Antibody, Biotin conjugated
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中文名稱:SLC35A2兔多克隆抗體, Biotin偶聯(lián)
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貨號:CSB-PA021584LD01HU
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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:Biotin
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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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應(yīng)用范圍:ELISA
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Protocols:
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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.
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:
- 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?。?/div>Congenital disorder of glycosylation 2M (CDG2M)亞細胞定位:Golgi apparatus membrane; Multi-pass membrane protein.蛋白家族:Nucleotide-sugar transporter family, SLC35A subfamily數(shù)據(jù)庫鏈接:
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