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5号染色体开放阅读框42抗体

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产品名称: 5号染色体开放阅读框42抗体
产品型号: C5ORF42
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

5号染色体开放阅读框42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。5号染色体开放阅读框42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。


5号染色体开放阅读框42抗体  的详细介绍

5号染色体开放阅读框42抗体

规格:1mg/1ml

英文名: C5ORF42

别名: Chromosome 5 open reading frame 42; FLJ13231; Hypothetical protein LOC65250; Transmembrane protein ENSP00000382582; Uncharacterized protein C5orf42; CE042_HUMAN.

分子量: 362kDa

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 C5ORF42

交叉反应:Human, Mouse, Rat, Dog, Cow, Sheep,

细胞定位:

5号染色体开放阅读框42抗体产品介绍:Subcellular Location: Membrane; Multi-pass membrane protein (Potential). DISEASE: Defects in C5orf42 are the cause of Joubert syndrome type 17 (JBTS17) [MIM:614615]. A disorder presenting with cerebellar ataxia, oculomotor apraxia, hypotonia, neonatal breathing abnormalities and psychomotor delay. Neuroradiologically, it is characterized by 5号染色体开放阅读框42抗体cerebellar vermian hypoplasia/aplasia, thickened and reoriented superior cerebellar peduncles, and an abnormally large interpeduncular fossa, giving the appearance of a molar tooth on transaxial slices (molar tooth sign). Additional 5号染色体开放阅读框42抗体variable features include retinal dystrophy and renal disease. Database links: Entrez Gene: 65250 Human SwissProt: Q9H799 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

5号染色体开放阅读框42抗体产品应用:ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1:20-500 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:细胞生物  **学  

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

来源: Rabbit


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