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19号染色体开放阅读框64/C19orf64抗体

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产品名称: 19号染色体开放阅读框64/C19orf64抗体
产品型号: GIPC3
产品展商: 单克隆抗体/多克隆抗体
产品文档: 无相关文档

简单介绍

19号染色体开放阅读框64/C19orf64抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。19号染色体开放阅读框64/C19orf64抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产品质量,质量稳定,实验效果明显。


19号染色体开放阅读框64/C19orf64抗体  的详细介绍

19号染色体开放阅读框64/C19orf64抗体

规格:1mg/1ml

英文名: GIPC3

别名: C19orf64; DKFZp686J1198; FLJ40925; GIPC 3; GIPC3_HUMAN ; GIPC PDZ domain containing family member 3; PDZ domain containing protein GIPC 3; PDZ domain containing protein GIPC3; PDZ domain protein GIPC

分子量: 34kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:Polyclonal

亚型:IgG

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human GIPC3

交叉反应:Human, Mouse, Rat, Dog, Cow,

细胞定位:

19号染色体开放阅读框64/C19orf64抗体产品介绍:background: The protein encoded by this gene belongs to the GIPC family. Studies in mice suggest that this gene is required for postnatal maturation of the hair bundle and long-term survival of hair cells and spiral ganglion in the ear. Mutations in this gene are associated with autosomal recessive deafness. [provided by RefSeq, Dec 2011] Function: GIPC3 is widely expressed in ***** and fetal tissues. Highest levels are found in jejunum, lymph node, parietal lobe, fetal spleen and fetal thymus. It is expressed in cervical, melanoma, chronic myelogenous and gastric cancer cell lines. Tissue Specificity: Widely expressed in ***** and fetal tissues.19号染色体开放阅读框64/C19orf64抗体 Highest levels are found in jejunum, lymph node, parietal lobe, fetal spleen and fetal thymus. Expressed in cervical, melanoma, chronic myelogenous and gastric cancer cell lines. DISEASE: Deafness, autosomal recessive, 15 (DFNB15) [MIM:601869]: A form of non-syndromic sensorineural hearing loss with prelingual onset. Sensorineural deafness results from damage to the neural receptors of the inner ear,19号染色体开放阅读框64/C19orf64抗体 the nerve pathways to the brain, or the area of the brain that receives sound information. Note=The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the GIPC family. Contains 1 PDZ (DHR) domain. Gene ID: 126326 Database links: Entrez Gene: 126326 Human Omim: 608792 Human SwissProt: Q8TF64 Human Unigene: 266873 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

19号染色体开放阅读框64/C19orf64抗体产品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:肿瘤  细胞生物  信号转导  G蛋白信号  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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