Anti-CCCCDC102B抗体CCDC102B is a 513 amino acid protein that exists as three alternatively spliced isoforms. Widely expressed and found in multiple CNV （copy-number variant）

产品编号 yb-7986R
英文名称 Anti-CCCCDC102B抗体
中文名称 卷曲螺旋结构域蛋白102B抗体
别    名 ACY1L; aminoacylase 1-like1; AN; C102B_HUMAN; C18orf14; CCDC102B; chromosome 18 open reading frame 14; coiled-coil domain containing 102B; Coiled-coil domain-containing protein 102B; DKFZp434K1426; DKFZp686I08254; FLJ23594; HsT1731; MGC161726; MGC161728.
 Anti-CCCCDC102B抗体  
说 明 书 0.2ml  
研究领域 细胞生物  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Sheep, 
产品应用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=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.
分 子 量 60kDa
性    状 Lyophilized or Liquid
浓    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human CCDC102B
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
 
PubMed PubMed
产品介绍 background:
CCDC102B is a 513 amino acid protein that exists as three alternatively spliced isoforms. Widely expressed and found in multiple CNV (copy-number variant) regions, CCDC102B contains the deletion breakpoint of a maternally inherited deletion, which is 2.7?Mb in size, and maps to human chromosome 18q22.1. CCDC102B may play a role in the pathogenesis of diaphragmatic hernia, microphthalmia, colorectal carcinoma and schizophrenia. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Translocation between chromosomes 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic angiectasia and erythropoietic protoporphyria are associated with chromosome 18

Database links:
UniProtKB/Swiss-Prot: Q68D86.4
 
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.