COG7 Antibody
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货号:CSB-PA005711GA01HU
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规格:¥3,900
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其他:
产品详情
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Uniprot No.:P83436
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基因名:COG7
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别名:CDG2E antibody; COG complex subunit 7 antibody; cog7 antibody; COG7_HUMAN antibody; Component of oligomeric Golgi complex 7 antibody; Conserved oligomeric Golgi complex component 7 antibody; Conserved oligomeric Golgi complex subunit 7 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 COG7
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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
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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.
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靶点详情
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功能:Required for normal Golgi function.
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基因功能参考文献:
- Cog5-Cog7 crystal structure reveals interactions essential for the function of a multisubunit tethering complex. PMID: 25331899
- COG5- and COG7 subunits play distinctive roles in controlling Golgi structure and function PMID: 16051600
- Retrograde transport of multiple Golgi proteins to the ER in COG-7-deficient patient fibroblasts via brefeldin A-induced tubules was significantly slower than occurs in normal fibroblasts. PMID: 16510524
- A homozygous, intronic splice site mutation (c.169+4A>C) of the COG7 gene was identified in 3 patients with Congenital Disorder of Glycosylation type IIe. PMID: 17356545
- A new mutation in COG7 extends the spectrum of COG subunit deficiencies. PMID: 19577670
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相关疾病:Congenital disorder of glycosylation 2E (CDG2E)
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亚细胞定位:Golgi apparatus membrane; Peripheral membrane protein.
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蛋白家族:COG7 family
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数据库链接:
HGNC: 18622
OMIM: 606978
KEGG: hsa:91949
STRING: 9606.ENSP00000305442
UniGene: Hs.185807
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