CT47B1,肿瘤/睾丸抗原47B1抗体

产品编号HZ-14094R
英文名称CT47B1
中文名称肿瘤/睾丸抗原47B1抗体
别 名cancer/testis antigen 47.13; cancer/testis antigen 47B; cancer/testis antigen family 47, member B1; cancer/testis CT47 family, member 13; CT47.13; CT47B_HUMAN; CT47A13.
说 明 书0.1ml 0.2ml
研究领域肿瘤 免疫学 肿瘤细胞生物标志物
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human,
CT47B1,肿瘤/睾丸抗原47B1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31kDa
细胞定位细胞核
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human CT47B1
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.
CT47B1,肿瘤/睾丸抗原47B1抗体PubMedPubMed
产品介绍background:
CT47 (cancer/testis antigen family 47) is a 288 amino acid protein that is strongly expressed in testis and lowly expressed in placenta and in brain. The gene encoding CT47 is located on human chromosome X, which 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.

Tissue Specificity:

DISEASE:

Gene ID:
643311

Database links:
Entrez Gene: 643311 Human
Omim: 300790 Human
SwissProt: P0C2W7 Human
Unigene: 729566 Human

CT47B1,肿瘤/睾丸抗原47B1抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.