Anti-C10orf93抗体C10orf93 , also known as C10orf124 or TPR repeat-containing protein C10orf93, is a 1,530 amino acid protein that contains two TPR

产品编号 yb-9772R
英文名称 Anti-C10orf93抗体
中文名称 10号染色体开放阅读框93抗体
别    名 C10orf124; C10orf93; Chromosome 10 open reading frame 93; CJ093_HUMAN; hypothetical protein LOC255352; TPR repeat-containing protein C10orf93.
Anti-C10orf93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, Cow, 
产品应用 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.
分 子 量 303kDa
性    状 Lyophilized or Liquid
浓    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human C10orf93
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:
C10orf93 , also known as C10orf124 or TPR repeat-containing protein C10orf93, is a 1,530 amino acid protein that contains two TPR repeats and exists as three alternatively spliced isoforms. The gene encoding C10orf93 maps to human chromosome 10q26.3. Spanning nearly 135 million base pairs, chromosome 10 makes up approximay 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.