CXorf59,X染色体开放阅读框59抗体

产品编号HZ-14120R
英文名称CXorf59
中文名称X染色体开放阅读框59抗体
别 名Chromosome X open reading frame 59; CHDC2_HUMAN; CXorf59; FLJ36601; Hypothetical protein LOC286464; MGC126747; MGC126749; OTTHUMP00000023134; RP13-11B7.1; Uncharacterized protein CXorf59.
说 明 书0.1ml 0.2ml
研究领域细胞生物 免疫学 发育生物学
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human,
CXorf59,X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58kDa
细胞定位细胞膜
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human CXorf59
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.
CXorf59,X染色体开放阅读框59抗体PubMedPubMed
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 CXorf59 gene product has been provisionally designated CXorf59 pending further characterization.

Subcellular Location:
Membrane.

Gene ID:
296464

Database links:
Entrez Gene: 286464 Human
SwissProt: Q8N9S7 Human
Unigene: 376425 Human

CXorf59,X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.