mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  人才招聘  關于我們  聯(lián)系我們
久久国产精品99久,日韩一区二区综合精品
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-CT47B1/Gold Conjugated antibody (bs-14094R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@www.p2b3.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.p2b3.cn
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產品編號 bs-14094R-Gold
英文名稱1 Rabbit Anti-CT47B1/Gold Conjugated antibody
中文名稱 膠體金標記的腫瘤/睪丸抗原47B1抗體
別    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.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 腫瘤  免疫學  腫瘤細胞生物標志物  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, )
產品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 31kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CT47B1
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產品介紹 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.

Database links:

Entrez Gene: 643311 Human

Omim: 300790 Human

SwissProt: P0C2W7 Human

Unigene: 729566 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.www.p2b3.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫(yī)療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
宝丰县| 齐河县| 丹江口市| 会昌县| 清涧县| 鸡泽县| 嘉义县| 禹州市| 泗阳县| 开江县| 鄂托克旗| 赤壁市| 芜湖县| 霍林郭勒市| 吉林市| 边坝县| 尚义县| 崇阳县| 光泽县| 普安县| 信丰县| 左权县| 手机| 余庆县| 乌兰察布市| 伊金霍洛旗| 肇源县| 平陆县| 光山县| 临湘市| 亳州市| 浑源县| 盘山县| 福建省| 鄂托克旗| 辉县市| 沅陵县| 平江县| 邯郸县| 沁阳市| 吉林市|