ALG12 Antibody
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中文名称:ALG12兔多克隆抗体
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货号:CSB-PA887130LA01HU
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规格:¥440
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促销:
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图片:
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) ALG12 Polyclonal antibody
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Uniprot No.:Q9BV10
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基因名:ALG12
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别名:6-mannosyltransferase antibody; ALG12 antibody; ALG12_HUMAN antibody; Asparagine linked glycosylation 12 alpha 1 6 mannosyltransferase homolog antibody; Asparagine linked glycosylation protein 12 homolog antibody; Asparagine-linked glycosylation protein 12 homolog antibody; CDG1G antibody; Dol P Man:Man(7)GlcNAc(2) PP Dol alpha 1 6 mannosyltransferase antibody; Dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1 antibody; Dolichyl P Man:Man(7)GlcNAc(2) PP dolichyl alpha 1 6 mannosyltransferase antibody; Dolichyl P mannose:Man 7 GlcNAc 2 PP dolichyl alpha 6 mannosyltransferase antibody; Dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichyl-alpha-1 antibody; ECM39 antibody; hALG12 antibody; Mannosyltransferase ALG12 homolog antibody; Membrane protein SB87 antibody; MGC111358 antibody; MGC3136 antibody; PP14673 antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human Dol-P-Man:Man (7)GlcNAc (2)-PP-Dol alpha-1,6-mannosyltransferase protein (367-422AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,ALG12 Antibody (CSB-PA887130LA01HU),的标记方式是Non-conjugated。对于ALG12 Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, IHC, IF
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推荐稀释比:
Application Recommended Dilution IHC 1:20-1:200 IF 1:50-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期: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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靶点详情
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功能:Adds the eighth mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2)) required for protein glycosylation.
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基因功能参考文献:
- deficiency results in congenital disorders of glycosylation type Ig PMID: 11983712
- this enzyme has a role in glycosylation and its deficiency causes congenital disorder of glycosylation type Ig PMID: 12093361
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相关疾病:Congenital disorder of glycosylation 1G (CDG1G)
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亚细胞定位:Endoplasmic reticulum membrane; Multi-pass membrane protein.
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蛋白家族:Glycosyltransferase 22 family
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组织特异性:Expressed in fibroblasts.
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数据库链接:
HGNC: 19358
OMIM: 607143
KEGG: hsa:79087
STRING: 9606.ENSP00000333813
UniGene: Hs.526711
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