PIGO Antibody
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货号:CSB-PA017978GA01HU
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规格:¥3,900
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其他:
产品详情
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Uniprot No.:Q8TEQ8
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基因名:
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别名:PIGO antibody; UNQ632/PRO1249 antibody; GPI ethanolamine phosphate transferase 3 antibody; EC 2.-.-.- antibody; Phosphatidylinositol-glycan biosynthesis class O protein antibody; PIG-O antibody
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宿主:Rabbit
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反应种属:Human,Mouse,Rat
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免疫原:Human PIGO
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免疫原种属:Homo sapiens (Human)
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抗体亚型:IgG
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纯化方式:Antigen Affinity 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:PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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产品提供形式:Liquid
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应用范围:ELISA,WB,IHC,IF
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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:Ethanolamine phosphate transferase involved in glycosylphosphatidylinositol-anchor biosynthesis. Transfers ethanolamine phosphate to the GPI third mannose which links the GPI-anchor to the C-terminus of the proteins by an amide bond.
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基因功能参考文献:
- PIGO deficiency shows variable phenotypes from infantile lethality to mild learning difficulties PMID: 28337824
- Disease associated PIGO missense mutations resulted in decreased activity in vitro. PMID: 28327575
- Novel PIGO mutations expand the clinical spectrum of PIGO abnormalities to include epileptic encephalopathy with mild elevation of alkaline phosphatase (ALP). PMID: 24417746
- Our data identify PIGO as the second gene associated with HPMRS and suggest that a deficiency in GPI-anchor synthesis is the underlying molecular pathomechanism of HPMRS. PMID: 22683086
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相关疾病:Hyperphosphatasia with mental retardation syndrome 2 (HPMRS2)
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亚细胞定位:Endoplasmic reticulum membrane; Multi-pass membrane protein.
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蛋白家族:PIGG/PIGN/PIGO family, PIGO subfamily
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数据库链接:
HGNC: 23215
OMIM: 614730
KEGG: hsa:84720
STRING: 9606.ENSP00000339382
UniGene: Hs.522099
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