亚洲制服欧美另类-午夜激情av电影-日本高清中文字幕一区二区三区-中国欧美日韩一区二区三区-欧洲亚洲日本韩国-成人欧美激情一区二区-亚洲偷偷自拍高清

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  關(guān)于我們  聯(lián)系我們
夜鲁夜鲁很鲁在线视频视频,精品国产午夜福利精品推荐,搡BBBB槡BBBB
Rabbit Anti-TPM2/BF555 Conjugated antibody (bs-1243R-BF555)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@bioss.com.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-1243R-BF555
英文名稱 Rabbit Anti-TPM2/BF555 Conjugated antibody
中文名稱 BF555標(biāo)記的原肌球蛋白抗體
別    名 AMCD1; Beta tropomyosin muscle; BETA-TM; DA1; DA2B; EPITHELIAL TROPOMYOSIN; FIBROBLAST MUSCLE TYPE TROPOMYOSIN; MGC109519; NEM4; TM2; TMSB; TPM2; TROP-2; TROPOMYOSIN 2; Tropomyosin 2 (beta chain); TPM2_MOUSE; TPM2_HUMAN.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說 明 書 100ul  
研究領(lǐng)域 腫瘤  細(xì)胞生物  信號(hào)轉(zhuǎn)導(dǎo)  細(xì)胞凋亡  細(xì)胞表面分子  細(xì)胞分化  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Chicken, Dog, Cow, Rabbit, )
產(chǎn)品應(yīng)用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 33kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human TPM2
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 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(chǎn)品介紹 background:
Tropomyosin is a dimeric coiled coil protein that binds along the length of actin filaments. It is associated with the thin filaments of muscle cells and the microfilaments of nonmuscle cells. Chicken embryo fibroblasts (CEF) contain five isoforms of tropomyosin (a, b, 1, 2, and 3), identified as such by their different apparent molecular masses after separation by SDS-PAGE, but similar biochemical properties, such as resistance to heat and organic solvents, the ability to bind to F actin filaments, and the lack of proline and tryptophan.

Function:
Binds to actin filaments in muscle and non-muscle cells. Plays a central role, in association with the troponin complex, in the calcium dependent regulation of vertebrate striated muscle contraction. Smooth muscle contraction is regulated by interaction with caldesmon. In non-muscle cells is implicated in stabilizing cytoskeleton actin filaments. The non-muscle isoform may have a role in agonist-mediated receptor internalization.

Subunit:
Heterodimer of an alpha and a beta chain.

Subcellular Location:
Cytoplasm, cytoskeleton.

Tissue Specificity:
Present in primary breast cancer tissue, absent from normal breast tissue.

Post-translational modifications:
Phosphorylated on Ser-61 by PIK3CG. Phosphorylation on Ser-61 is required for ADRB2 internalization.

DISEASE:
Nemaline myopathy 4 (NEM4) [MIM:609285]: A form of nemaline myopathy. Nemaline myopathies are muscular disorders characterized by muscle weakness of varying severity and onset, and abnormal thread-like or rod-shaped structures in muscle fibers on histologic examination. Nemaline myopathy type 4 presents from infancy to childhood with hypotonia and moderate-to-severe proximal weakness with minimal or no progression. Major motor milestones are delayed but independent ambulation is usually achieved, although a wheelchair may be needed in later life. Note=The disease is caused by mutations affecting the gene represented in this entry.
Arthrogryposis, distal, 1A (DA1A) [MIM:108120]: A form of distal arthrogryposis, a disease characterized by congenital joint contractures that mainly involve two or more distal parts of the limbs, in the absence of a primary neurological or muscle disease. Distal arthrogryposis type 1 is characterized largely by camptodactyly and clubfoot. Hypoplasia and/or absence of some interphalangeal creases is common. The shoulders and hips are less frequently affected. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the tropomyosin family.

Database links:

Entrez Gene: 7169 Human

Entrez Gene: 22004 Mouse

Entrez Gene: 500450 Rat

Omim: 190990 Human

SwissProt: P07951 Human

SwissProt: P58774 Mouse

SwissProt: P58775 Rat

Unigene: 300772 Human

Unigene: 646 Mouse

Unigene: 17580 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

Trop-2蛋白主要存在于細(xì)胞胞質(zhì)及表面, 它是絲裂原活化蛋白激酶(MAPK)通路的一個(gè)重要組成部,參與細(xì)胞生長(zhǎng)、增殖、分化、死亡及細(xì)胞間的功能同步等多種生理過程.
Trop-2在很多常見的腫瘤上扮演著重要角色,其中包括乳腺癌、胃癌、結(jié)腸癌、肺癌、前列腺癌、胰腺癌和子宮癌,有學(xué)者認(rèn)為:Trop-2在孕期內(nèi)所具有的生殖功能可能意味著它同腫瘤的生長(zhǎng)有關(guān)聯(lián)。
版權(quán)所有 2004-2026 a6308.cn 北京博奧森生物技術(shù)有限公司
通過國(guó)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(guó)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)
国产一级Av片在线观看 | 国产精品久久久久久亚洲影视 | 国产精品久久久久久精品爆乳 | 亚洲国产精品VA在线看黑木耳 | 亚洲欧洲日产国产 最新 | 欧美一区二区三区不卡免费 | 人妻插B视频一区二区三区 久爱成欢视频在线观看 | 日韩亚洲人成网站在线播放 | 欧美日韩永久久一区二区三区 | 最新日韩中文字幕 | 夜夜爱成人免费网站 | 国产AVXXXX无套内射 | 日韩美女乱淫试看屁视频网站 | 最近最新免费手机中文 | 欧美日韩一区二区三区自拍 | 亚洲乱码日产精品BD在线看 | 久久99国产精品一区二区 | 成人免费无遮挡无码黄漫视频 | 国产无遮挡成人免费视频网站 | 人人妻人人添人人爽欧美一区91 | 一区二区三区国模大胆 | 色婷婷国产精品无码视频 | 亚洲欧美一区二区成人片 | 国产免费看JIZZ视频 | 久久久久久精品毛片A级按摩 | 91精品国产色综合久久不卡美美 | 国产欧美日韩在线精品 | 乱码视频午夜在线观看 | 国偷自产一区二区免费 | 国产91成人精品流白浆 | 夜夜躁狠狠躁日日躁2022 | 日韩精品福利视频一区二区三区 | 免费精品美女久久久久久久久久 | 毛片线看免费观看 | 亚洲黄色网站免费观看 | 无码专区—va亚洲v专区 | 欧美人妻精品一区二区三区 | 欧美一区二区三区久久综 | 国产精品无码久久久最线观看 | 国产精品日本欧美一区二区 | 久久久国产精品免费看 |