C5orf22,5号染色体开放阅读框22抗体

产品编号HZ-15200R
英文名称C5orf22
中文名称5号染色体开放阅读框22抗体
别 名UPF0489 protein C5orf22; C5orf22; CE022_HUMAN.
说 明 书0.1ml 0.2ml
研究领域细胞生物 免疫学 染色质和核信号
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human, Mouse, Rat, Dog,
C5orf22,5号染色体开放阅读框22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.
分 子 量50kDa
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human C5orf22
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.
C5orf22,5号染色体开放阅读框22抗体PubMedPubMed
产品介绍background:
With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf22 gene product has been provisionally designated C5orf22 pending further characterization.

Similarity:
Belongs to the UPF0489 family.

Database links:
Entrez Gene: 55322 Human
SwissProt: Q49AR2 Human
Unigene: 519246 Human

C5orf22,5号染色体开放阅读框22抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.