C9orf98,9号染色体开放阅读框98抗体

产品编号HZ-15351R
英文名称C9orf98
中文名称9号染色体开放阅读框98抗体
别 名adenylate kinase 8; chromosome 9 open reading frame 98; DDX31; Putative adenylate kinase like protein C9orf98; putative adenylate kinase-like protein C9orf98; KAD8_HUMAN.
说 明 书0.1ml 0.2ml
研究领域细胞生物 免疫学 信号转导 新陈代谢
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human,
C9orf98,9号染色体开放阅读框98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55kDa
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human C9orf98
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.
C9orf98,9号染色体开放阅读框98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 C9orf98 gene maps to human chromosome 9q34.13. Consisting of 479 amino acids, C9orf98 exists as two alternatively spliced isoforms and belongs to the adenylate kinase family.

Function:
Adenylate kinase. Has highest activity toward AMP, and weaker activity toward dAMP, CMP and dCMP.

Subcellular Location:
Cytoplasm, cytosol.

Similarity:
Belongs to the adenylate kinase family.

Database links:
Entrez Gene: 158067 Human
SwissProt: Q96MA6 Human

C9orf98,9号染色体开放阅读框98抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.