中文名称

FAM73B蛋白抗体

别    名

C9orf54; FA73B_HUMAN; Fam73b; Family   with sequence similarity 73, member B; FLJ00199; FLJ14596; Protein FAM73B;   RP11-167N5.1.  

抗体来源

Rabbit

克隆类型

Polyclonal

交叉反应

Human,  (predicted:   Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )

产品应用

WB=1:500-2000 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.

理论分子量

65kDa

细胞定位

细胞浆 

性    状

Liquid

浓    度

1mg/ml

免 疫 原

KLH conjugated synthetic peptide   derived from human FAM73B: 51-150/593 

亚    型

IgG

纯化方法

affinity purified by Protein A

缓 冲 液

0.01M TBS(pH7.4) with 1% BSA, 0.03%   Proclin300 and 50% Glycerol.

保存条件

Shipped at 4℃. Store at -20 °C for one year. Avoid repeated   freeze/thaw cycles.

注意事项

This product as supplied is intended   for research use only, not for use in human, therapeutic or diagnostic   applications.

产品介绍

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 FAM73B gene product has been provisionally   designated FAM73B pending further characterization.