日日操日日操,亚洲日本午夜激情,人妻内射精品一区二区,国产一区北条麻妃

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
国产超碰成人AV,情爱视频久久久
Rabbit Anti-TPM2/PE-Cy5 Conjugated antibody (bs-1243R-PE-Cy5)
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(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-1243R-PE-Cy5
英文名稱(chēng) Rabbit Anti-TPM2/PE-Cy5 Conjugated antibody
中文名稱(chēng) PE-Cy5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) (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(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.bklrv.cn 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)
弄久久又久久久| 国产精品第一区第一页| 欧美综合一区亚洲综合一区| 日韩H图片一区| 睡觉视频啊啊啊好爽好大操我| 日韩AⅤ黄五月天| 激情久久五月天无码-性做久久| 五月丁香激情澎湃无码| 最新欧美日韩成人一区二区| 国产未亡人一区二区| 久久久久人妻一区精品色| 日本wwwxxx,国产精品久久久| 久久久午夜伦理免费| 91人妻人人搡人人爽人人精品| 日本精品三级久久| 大香蕉一人综合| 亚洲美女国产综合| 色婷婷亚洲视频| 日本一区二区不卡a| 收看成人菊花视頻| 亚洲第一性交| 天天更新不卡精品一区| 亚洲欧洲无码不卡视频在线| 97视频在线观看| 国产经典久久久久久久六区| 欧洲亚洲人妻中文一区二区| 精品人妻在线无码视频| JJ一区二区中文字幕免费| 欧美日韩中文在线另 | 久久先锋超碰| 久久久强奸日本熟女| 试看视频免费| 大香蕉久久久| 亚洲AV大型| 欧美一级日韩一级亚洲一级| 日韩欧美中文字幕青青操| 91在线无码精品秘 少萝| 伦理导航香蕉| 91精品美女国产网站| 亚洲精品女教师在线观看| 国产精品自拍视频听|