C9orf59,9号染色体开放阅读框59抗体

产品编号HZ-9656R
英文名称C9orf59
中文名称9号染色体开放阅读框59抗体
别 名C9orf59; Chromosome 9 open reading frame 59; Family with sequence similarity 78, member A; FLJ00024; Hypothetical protein LOC286336;FAM78A.
说 明 书0.1ml 0.2ml
研究领域肿瘤 细胞生物 神经生物学
抗体来源Rabbit
克隆类型Polyclonal
交叉反应 Human, Mouse, Rat, Pig, Rabbit,
C9orf59,9号染色体开放阅读框59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32kDa
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human FAM78A/C9orf59
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.
C9orf59,9号染色体开放阅读框59抗体PubMedPubMed
产品介绍background:
Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The FAM78A gene product has been provisionally designated FAM78A pending further characterization.

Similarity:
Belongs to the FAM78 family.

Database links:
Entrez Gene: 286336 Human
Entrez Gene: 241303 Mouse
Entrez Gene: 499776 Rat
SwissProt: Q5JUQ0 Human
SwissProt: Q8C552 Mouse

C9orf59,9号染色体开放阅读框59抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.