CPA6 Antibody
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) CPA6 Polyclonal antibody
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Uniprot No.:Q8N4T0
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基因名:CPA6
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别名:CPA6 antibody; CPAHCarboxypeptidase A6 antibody; EC 3.4.17.- 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 Carboxypeptidase A6 protein (130-437AA)
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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,CPA6 Antibody (CSB-PA005880LA01HU),的标记方式是Non-conjugated。对于CPA6 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
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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:May be involved in the proteolytic inactivation of enkephalins and neurotensin in some brain areas. May convert inactive angiotensin I into the biologically active angiotensin II. Releases a C-terminal amino acid, with preference for large hydrophobic C-terminal amino acids and shows only very weak activity toward small amino acids and histidine.
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基因功能参考文献:
- Common variants in PRPF31 and CPA6 were associated with worse and better metformin response, respectively. PMID: 29650774
- these mutations in CPA6 are deleterious and provide further evidence for the involvement of CPA6 mutations in the predisposition for several types of epilepsy. PMID: 25875328
- Significantly higher levels of DNA methylation are found in the CPA6 promoter in focal epilepsy and febrile seizure patients. PMID: 24290490
- These results provide further evidence for the involvement of CPA6 mutations in human epilepsy. PMID: 23105115
- CPA6 mutatins are genetically linked to an autosomal recessive familial form of febrile seizures and temporal lobe epilepsy (TLE), and are associated with sporadic TLE cases. PMID: 21922598
- Substrate specificity of human carboxypeptidase A6 PMID: 20855895
- The CPAH gene was interrupted in a patient with DURS carrying a translocation break point in the DURS1 region on chromosome 8q13. PMID: 12454025
- CPA6 may have a role in the regulation of neuropeptides in the extracellular environment within the olfactory bulb and other parts of the brain PMID: 18178555
- Thrombin activation of osteopontin (OPN) (resulting in OPN-R) and its subsequent inactivation by thrombin-activatable carboxypeptidase B (generating OPN-L) occurs locally within inflamed joints in rheumatoid arthritis. PMID: 19790060
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相关疾病:Epilepsy, familial temporal lobe, 5 (ETL5); Febrile seizures, familial, 11 (FEB11)
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亚细胞定位:Secreted, extracellular space, extracellular matrix.
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蛋白家族:Peptidase M14 family
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组织特异性:Expressed in the hippocampus, nucleus raphe, and cortex.
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数据库链接:
HGNC: 17245
OMIM: 609562
KEGG: hsa:57094
STRING: 9606.ENSP00000297770
UniGene: Hs.658850
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