亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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  聯系我們
国产精品亚洲精品日韩已满,免费无码一区二区三区蜜桃大,日韩精品一区二区三区色欲av
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Phospho-HER3 (Tyr1197)/BF488 Conjugated antibody (bs-3218R-BF488)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-3218R-BF488
英文名稱1 Rabbit Anti-Phospho-HER3 (Tyr1197)/BF488 Conjugated antibody
中文名稱 BF488標記的磷酸化HER3抗體
別    名 Her3/ErbB3(phospho-Tyr1197); p-HRE3 (Tyr1197); ErbB 3 (phospho Y1197); ERBB3; c erbB 3; c erbB3; ERBB3 protein; erbB3 S; Glial growth factor receptor; HER 3; HER3; LCCS2; MDA BF 1; MGC88033; p180 ErbB3; p45 sErbB3; p85 sErbB3; proto-oncogene-like protein c ErbB 3; proto-oncogene-like protein c ErbB3; receptor tyrosine protein kinase ERB3; Receptor tyrosine protein kinase erbB 3; Receptor tyrosine protein kinase erbB3; Tyrosine kinase type cell surface receptor HER3; ERBB3_HUMAN.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
產品類型 磷酸化抗體 
研究領域 腫瘤  免疫學  信號轉導  生長因子和激素  激酶和磷酸酶  細胞膜受體  G蛋白偶聯受體  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, Mouse, Rat, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 148kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated Synthesised phosphopeptide derived from human HER3 around the phosphorylation site of Tyr1197 [EE(p-Y)EY]
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol
保存條件 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.
產品介紹 background:
ErbB3 is a member of the epidermal growth factor receptor (EGFR) family of receptor tyrosine kinases. ErbB3 is a membrane-bound protein which has a neuregulin binding domain but not an active kinase domain. It can therefore bind this ligand but cannot convey a signal into the cell via protein phosphorylation. However it does form heterodimers with other EGF receptor family members which do have kinase activity. Heterodimerization leads to the activation of pathways which lead to cell proliferation or differentiation. Amplification of this gene and/or overexpression of its protein have been reported in numerous cancers including prostate, bladder and breast tumors. Alternate transcriptional splice variants encoding different isoforms have been characterized. Isoform 2 lacks the intermembrane region and is secreted outside the cell. This form acts to modulate the activity of the membrane-bound form. Additional splice variants have also been reported but they have not been thoroughly characterized. Defects in ERBB3 are the cause of lethal congenital contracture syndrome type 2 (LCCS2); also called Israeli Bedouin multiple contracture syndrome type A. LCCS2 is an autosomal recessive neurogenic form of a neonatally lethal arthrogryposis that is associated with atrophy of the anterior horn of the spinal cord.

Function:
Binds and is activated by neuregulins and NTAK.

Subunit:
Monomer and homodimer. Heterodimer with each of the other ERBB receptors (Potential). Interacts with CSPG5, PA2G4, GRB7 and MUC1.

Subcellular Location:
Isoform 1: Cell membrane; Single-pass type I. membrane protein. Isoform 2: Secreted.

Tissue Specificity:
Epithelial tissues and brain.

Post-translational modifications:
Ligand-binding increases phosphorylation on tyrosine residues and promotes its association with the p85 subunit of phosphatidylinositol 3-kinase. Subject to autophosphorylation.

DISEASE:
Defects in ERBB3 are the cause of lethal congenital contracture syndrome type 2 (LCCS2) [MIM:607598]; also called Israeli Bedouin multiple contracture syndrome type A. LCCS2 is an autosomal recessive neurogenic form of a neonatally lethal arthrogryposis that is associated with atrophy of the anterior horn of the spinal cord. The LCCS2 syndrome is characterized by multiple joint contractures, anterior horn atrophy in the spinal cord, and a unique feature of a markedly distended urinary bladder. The phenotype suggests a spinal cord neuropathic etiology.

Similarity:
Belongs to the protein kinase superfamily. Tyr protein kinase family. EGF receptor subfamily.
Contains 1 protein kinase domain.

Database links:

Entrez Gene: 2065 Human

Entrez Gene: 13867 Mouse

Entrez Gene: 29496 Rat

Omim: 190151 Human

SwissProt: P21860 Human

SwissProt: Q61526 Mouse

SwissProt: Q62799 Rat

Unigene: 118681 Human

Unigene: 373043 Mouse

Unigene: 10228 Rat



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.chomd.com.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
主站蜘蛛池模板: 日本法律入室抢劫| 亚洲中文综合无码91| 大学生一级毛片免费看真人| 一级毛片视频播放最新片| 亚洲精品国精品久久99热,亚洲精品无码| 2021国产麻豆剧果冻传媒入口爱情公寓 | 亚洲精品国产综合久久一线_精 | 无码人妻精品字幕视频| 亚洲另类无码专区丝袜,一线产区二线生产区的| 99热门精品一区二区三区无码久久I精品| 亚洲白虎一区二区精品网站| 亚洲中文久久精品无码^99热国产| 全部免费毛片在线播放,美女大黄大色一级特| 中文字幕日产每天更新40亚欧黄片无码中文字幕 | 亚洲爆乳精品无码一区二区喷奶 | 国产免费内射又粗又爽密桃视频无码 | 一本在线不卡视频二区| 日韩三级在线观看视频.欧美精品日韩| 国产成人精品亚洲精品密臀| 国产区图片区小说区亚洲区妓女| 亚洲成a人片在线观看国产,青青视频| 最新国产成人精品视频地址| 中国老熟女重囗味HDXX| 亚洲中文无码免费论坛爱情岛| 站长工具人妻av日韩少妇| 日产精密秘?入口麻豆29| а√最新版天堂资源在线小说| 伸手进去?的我好爽无码| 日本孕妇孕交videostv| 97精品国产97久久久久久免费 | 久久久久久亚洲精品成人,亚洲日韩乱码久久 | 日韩人妻中文在线视频免费视频| 新版天堂资源中文8在线,操碰在线视频 | 国产精自产拍久久久久久蜜牛牛| 国语自产少妇精品视频_国产99久久久 | 精品国偷自产在线91,天| 丝袜精品一区二区视频| 免费观看一区二区三区网址大全 | 人人揉人人模AV国产 | 精品国产一区二区25P| 樱桃免费高清中文字幕视频网站|