ALG2 Antibody
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货号:CSB-PA314311
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规格:¥1100
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图片:
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The image on the left is immunohistochemistry of paraffin-embedded Human gastic cancer tissue using CSB-PA314311(ALG2 Antibody) at dilution 1/35, on the right is treated with fusion protein. (Original magnification: ×200)
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The image on the left is immunohistochemistry of paraffin-embedded Human lung cancer tissue using CSB-PA314311(ALG2 Antibody) at dilution 1/35, on the right is treated with fusion protein. (Original magnification: ×200)
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其他:
产品详情
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Uniprot No.:Q9H553
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基因名:ALG2
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别名:ALG2; UNQ666/PRO1298; Alpha-1,3/1,6-mannosyltransferase ALG2; Asparagine-linked glycosylation protein 2 homolog; GDP-Man:Man(1GlcNAc(2-PP-Dol alpha-1,3-mannosyltransferase; GDP-Man:Man(1GlcNAc(2-PP-dolichol mannosyltransferase; GDP-Man:Man(2GlcNAc(2-PP-Dol alpha-1,6-mannosyltransferase
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宿主:Rabbit
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反应种属:Human,Mouse
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免疫原:Fusion protein of Human ALG2
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
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抗体亚型:IgG
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纯化方式:Antigen affinity purification
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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:-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
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产品提供形式:Liquid
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应用范围:ELISA,IHC
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推荐稀释比:
Application Recommended Dilution ELISA 1:2000-1:5000 IHC 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.
相关产品
靶点详情
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功能:Mannosylates Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate.
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基因功能参考文献:
- We identify ALG14 and ALG2 as novel genes in which mutations cause a congenital myasthenic syndrome PMID: 23404334
- The ALG2 binding site is necessary for the punctate distribution of the carboxyl-terminal proline-rich region of Alix in HeLa cells. PMID: 14999017
- The expression and transport of ALG-2 in association with TSG101 and Vps4B are reported. PMID: 16004603
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相关疾病:Congenital disorder of glycosylation 1I (CDG1I); Myasthenic syndrome, congenital, 14 (CMS14)
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亚细胞定位:Membrane; Single-pass membrane protein.
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蛋白家族:Glycosyltransferase group 1 family, Glycosyltransferase 4 subfamily
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数据库链接:
HGNC: 23159
OMIM: 607905
KEGG: hsa:85365
STRING: 9606.ENSP00000417764
UniGene: Hs.40919
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