强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
掃碼關(guān)注公眾號(hào)           掃碼咨詢(xún)技術(shù)支持           掃碼咨詢(xún)技術(shù)服務(wù)
  
客服熱線(xiàn):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
少妇搡BBBB搡BBB搡失恋 ,久久免费精品视频
Rabbit Anti-TPM2/BF594 Conjugated antibody (bs-1243R-BF594)
訂購(gòu)熱線(xiàn):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(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢(xún)價(jià)
產(chǎn)品編號(hào) bs-1243R-BF594
英文名稱(chēng) Rabbit Anti-TPM2/BF594 Conjugated antibody
中文名稱(chēng) BF594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(mǎi)        大包裝/詢(xún)價(jià)
說(shuō) 明 書(shū) 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(lái)源 Rabbit
克隆類(lèi)型 Polyclonal
交叉反應(yīng)
產(chǎn)品應(yīng)用 ICC=1:50-200 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(guò)程.
Trop-2在很多常見(jiàn)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 m.nmgps.com 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書(shū)編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書(shū)編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
亚洲AV乱码一区二区三区老胖妞 | 欧美激情午夜精品久久久久久久久 | 91情趣福利姬在线观看 | 日韩丝袜人妻 中文字幕 | 久久丫精品久久丫 | 性猛交乱婬AV大片三級韩国理伦 | 懂色AV 粉嫩AV 蜜乳AV | 性一交一乱一色一免费无遮挡 | 中文字幕在线免费观看网站 | 在线观看黄色视频网站 | 色婷婷wAV秘 一区二区 | 在线观看免费无码视频 | 熟妇~x88AV海角社区 | 9l视频自拍蝌蚪9l成人 | 国产+无码+精品十欧美 | 91无码人妻精品一区 | 成人做爰A片一区二区 | 高清无码视频在线观看 | 国产中文字幕在线观看 | 国产精品一区二区视频 | 亚洲精品婷婷无码AV片带乳环 | 91人妻五码一区二区三区 | 国产睡熟迷奷系列精品视频 | 日本a片永久免费观看网站 快灬快灬 一下爽蜜桃日本 | 国产裸体舞一区二区三区婚闹 | 日本无码A片免费网站 | 少妇搡bbbb搡bbb| 蜜臀久久99精品久久久无需会员 | 国内大量偷窥精品视频 | 五月天婷亚洲天综合网综合 | 少妇又紧又色又爽又刺激视频 | 国产又粗又猛又黄又爽 | 小辣椒成人福利A∨导航 | 亚洲国产精品综合久久99视频 | 91人妻系列绿帽精品蜜臀 | 综合久久国产九一剧情麻豆 | 免费无码婬片AAAAA片 | 巨大乳人妻中文字幕 | 在线免费观看无码视频 | 欧洲美女自慰在线观看免费播放器 | 无码A片全身按摩AⅤ |