C2orf24,2号染色体开放阅读框24抗体

产品编号HZ-9804R
英文名称C2orf24
中文名称2号染色体开放阅读框24抗体
别 名CDABP0125; CGI 57; chromosome 2 open reading frame 24; CNPD1_HUMAN; CNPPD1; Cyclin Pas1/PHO80 domain-containing protein 1; Protein CNPPD1.
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, Chicken, Dog, Pig, Cow, Horse, Sheep,
C2orf24,2号染色体开放阅读框24抗体产品应用WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 IEM=1:20-200 IGS=1:20-200 GICA=1:20-200 （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45kDa
细胞定位细胞膜
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human C2orf24
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.
C2orf24,2号染色体开放阅读框24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 C2orf24 gene product has been provisionally designated C2orf24 pending further characterization.

Subcellular Location:
Membrane; Single-pass membrane protein (Potential).

Similarity:
Belongs to the CNPPD1 family.

Database links:
Entrez Gene: 27013 Human
Entrez Gene: 69171 Mouse
Entrez Gene: 316530 Rat
SwissProt: Q5E9J2 Cow
SwissProt: Q9BV87 Human
SwissProt: Q8K158 Mouse
SwissProt: Q6P7B2 Rat
Unigene: 4973 Human
Unigene: 28193 Mouse
Unigene: 101111 Rat

C2orf24,2号染色体开放阅读框24抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.