Deleted in autism 1 related protein; DIA1R; EPQL1862; hCG_1981635; hCG1981635; PRO3743; UPF0672 protein CXorf36; chromosome X open reading frame 36, isoform CRA_a; uncharacterized protein Cxorf36 precursor; PRO3743; EPQL1862; FLJ14103; FLJ55198; FLJ55198,; bA435K1.1; 4930578C19Rik; DKFZp313K0825; DIA1R_HUMAN; CXorf36.
规格价格
100ul/2980元 购买 大包装/询价
说 明 书
100ul
研究领域
免疫学
抗体来源
Rabbit
克隆类型
Polyclonal
交叉反应
Human, Mouse,
产品应用
IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
分 子 量
45kDa
性 状
Lyophilized or Liquid
浓 度
1mg/ml
免 疫 原
KLH conjugated synthetic peptide derived from human CXorf36
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.
产品介绍
background: The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXorf36 gene product has been provisionally designated CXorf36 pending further characterization.
Subcellular Location: Secreted (Potential).
DISEASE: Note=Genetic variations in CXorf36 may be associated with susceptibility to autism.
Similarity: Belongs to the DIA1 family.
Database links:
Entrez Gene: 79742 Human
SwissProt: Q9H7Y0 Human
Unigene: 98321 Human
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.