吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

掃碼關(guān)注公眾號(hào)           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  人才招聘  關(guān)于我們  聯(lián)系我們
黑人大荫道BBWBBB高潮潮喷,偷窥美女洗澡一区二区三区
Rabbit Anti-Phospho-HER3 (Tyr1289)/Gold Conjugated antibody (bs-3491R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-3491R-Gold
英文名稱1 Rabbit Anti-Phospho-HER3 (Tyr1289)/Gold Conjugated antibody
中文名稱 膠體金標(biāo)記的磷酸化HER3抗體
別    名 Her3/ErbB3(phospho-Tyr1289); p-HRE3 (Tyr1289); ErbB 3 (phospho Y1289); 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(guī)格價(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
說 明 書 100ul(10nm  15nm  35nm
產(chǎn)品類型 磷酸化抗體 
研究領(lǐng)域 腫瘤  細(xì)胞生物  免疫學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  細(xì)胞凋亡  生長因子和激素  轉(zhuǎn)錄調(diào)節(jié)因子  細(xì)胞膜受體  腫瘤細(xì)胞生物標(biāo)志物  跨膜蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Mouse, Rat,  (predicted: Human, Dog, Cow, Horse, Rabbit, )
產(chǎn)品應(yīng)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 148kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated Synthesised phosphopeptide derived from human HER3 around the phosphorylation site of Tyr1289 [QG(p-Y)EE]
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 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(chǎn)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(quán)所有 2004-2026 www.xucheq.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號(hào): 00124Q34771R2M/1100
通過國際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
国产精品丝袜久久久久久不卡| 亚洲人成网站999久久久综合| 女人张开腿让男人桶爽| 国产精品无码专区| 肥嫩多毛的大荫户| 国产精品无码免费播放| 欧美成人一区二区三区| 被喂春药蹂躏的欲仙欲死视频| 亚洲日韩精品一区二区三区| 实拍各种胸走光见奶头| 国产成人精品久久| 国产精品国色综合久久| 久久久久久AV无码免费看大片 | 亚洲午夜久久久久久久久电影网| 高清视频在线观看| 无码久久精品国产亚洲AV影片| 亚洲国产精久久久久久久| 丰满的人妻hd高清日本| 成人亚洲区无码偷拍12P| 老头扒开粉嫩的小缝亲吻| CHINESE老女人老熟妇| 日本又色又爽又黄的A片18禁| 51精产一二三产区区别| 国产成人一区二区三区| 一次灌浆与二次灌浆| 国产中年熟女高潮大集合| 中文字幕精品久久久久人妻 | 国产成人无码A区在线观看导航 | 欧美精产国品一二三产品区别在哪 | 国产日产久久高清欧美一区| 色戒完整版| 国产SUV精二区九色| 久久精品亚洲一区二区三区浴池 | 人妻AV无码一区二区三区| 精品亚洲麻豆1区2区3区| 97精品国产一区二区三区| 国产精品秘入口18禁麻豆免会员| 成人H动漫精品一区二区无码| 国产无遮挡又黄又爽在线观看| 精品久久久久久综合日本| 秋霞成人午夜鲁丝一区二区三区 |