C2orf63,2号染色体开放阅读框63抗体

产品编号HZ-16119R
英文名称C2orf63
中文名称2号染色体开放阅读框63抗体
别 名FLJ31438; C2orf63; CLHC1_HUMAN; Chromosome 2 open reading frame 63; Hypothetical protein LOC130162.
说 明 书0.1ml 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, Pig, Horse,
C2orf63,2号染色体开放阅读框63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67kDa
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human C2orf63
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 癈 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癈. 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 癈.
C2orf63,2号染色体开放阅读框63抗体PubMedPubMed
产品介绍background:
The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The FLJ31438 gene product has been provisionally designated FLJ31438 pending further characterization.

Function:
FLJ31438 is a putative uncharacterized protein.

Gene ID:
130162

Database links:
Entrez Gene: 130162 Human
SwissProt: Q8NHS4 Human

C2orf63,2号染色体开放阅读框63抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.