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Rabbit Anti-CXorf36/BF350 Conjugated antibody (bs-0488R-BF350)
~~~促销,代码KXJ230206-6~~~
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说 明 书: 100ul  
100ul/2980.00元
大包装/询价
产品编号 bs-0488R-BF350
英文名称 Anti-CXorf36/BF350
中文名称 BF350标记的脱羧酶蛋白体36抗体
别    名 chromosome X open reading frame 36, isoform CRA_a ; uncharacterized protein Cxorf36 precursor; PRO3743; EPQL1862; FLJ14103; FLJ55198; FLJ55198, bA435K1.1; 4930578C19Rik; DKFZp313K0825; CXorf36; DIA1R_HUMAN; DIA1R; PRO3743; EPQL1862; bA435K1.1; 4930578C19Rik.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 肿瘤  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human,  (predicted: Mouse, Rat, Dog, Cow, )
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 20/45kDa
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.

经研究:CXorf36蛋白是通过其水解酶活性,在肿瘤的发生、生长或侵袭过程中发挥重要作用。对关于CXorf36基因功能的研究,其在肿瘤组织中的定位、对细胞生物学功能的影响需进一步研究。

文献参考: 肾癌相关基因CXorf36的克隆及亚定位研究
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