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1号染色体开放阅读框96抗体

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产物名称: 1号染色体开放阅读框96抗体
产物型号: C1orf96
产物展商: 单克隆抗体/多克隆抗体
产物文档: 无相关文档

简单介绍

1号染色体开放阅读框96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。1号染色体开放阅读框96抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产物质量,质量稳定,实验效果明显。


1号染色体开放阅读框96抗体  的详细介绍

1号染色体开放阅读框96抗体

规格:1尘驳/1尘濒

英文名: C1orf96

别名: C1orf96; FLJ37296; FLJ41471; Uncharacterized protein C1orf96; CCSAP_HUMAN; Centriole, cilia and spindle-associated protein; CCSAP; CSAP; RP4-803J11.3.

分子量: 30kDa

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

克隆类型:笔辞濒测肠濒辞苍补濒

亚型:滨驳骋

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human C1orf96

交叉反应:Human, Mouse, Rat, Chicken, Dog, Horse, Rabbit,

细胞定位:细胞浆

1号染色体开放阅读框96抗体产物介绍:background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The 1号染色体开放阅读框96抗体C1orf96 gene product has been provisionally designated C1orf96 pending further characterization. Function: May play a role in embryonic development. May be required for proper cilia beating. Subunit: Associates with microtubules; the association occurs on polyglutamylated tubulin. Subcellular Location: Cytoplasm, cytoskeleton, centrosome, centriole. Cytoplasm, cytoskeleton, spindle. Cytoplasm, cytoskeleton. Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton, cilium axoneme. Cell projection, axon. Cell projection, cilium. Note=Localizes 1号染色体开放阅读框96抗体to two to four centrioles throughout the cell cycle. Localizes to mitotic spindle microtubules during prometaphase and throughout the remainder of mitosis. Localizes to cytoskeleton on interphase. Localizes at the ciliary transition zone which connects the basal bodies to ciliary microtubules. Colocalizes with polyglutamylated tubulin. Similarity: Belongs to the CCSAP family. Database links: Entrez Gene: 126731 Human SwissProt: Q6IQ19 Human Unigene: 725991 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

1号染色体开放阅读框96抗体产物应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (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  **学  

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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