来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

掃碼關(guān)注公眾號           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
99国产精品国产精品九九|亚洲中文字体无码AV网址|晚上看B站直播APP
Rabbit Anti-TPM2/Biotin Conjugated antibody (bs-1243R-Bio)
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@73327.net
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-1243R-Bio
英文名稱1 Rabbit Anti-TPM2/Biotin Conjugated antibody
中文名稱 生物素標(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)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 腫瘤  細(xì)胞生物  信號轉(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 WB=1:50-200 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=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 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)通路的一個重要組成部,參與細(xì)胞生長、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有關(guān)聯(lián)。
版權(quán)所有 2004-2026 www.73327.net 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: 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: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網(wǎng)安備110107000727號
熟妇人妻久久中文字幕| 色噜噜亚洲一本在线视频| 免费的视频APP网站| 日本在线观看| 三级三码视频在线播放| 成年片人免费红杏直播| 波多野结衣电影| 2020国产精品久久精品不卡| 少妇扒开粉嫩小泬视频| 久久久久久久久久女黄久久久久久 | 老司机午夜视频十八福利| 小荡货奶真大水多好紧视频| 久久综合伊人77777| 成人精品视频99在线观看免费| 黑人太大了太深了好痛 视频| 亚洲日韩一区二区三区| 亚洲AV无码乱码在线观看富二代| 欧美极品少妇×XXXBBB| 精品久久在线一区二区| 国产精品爽黄69天堂A片| 亚洲a∨一区二区三区性色 | 精精国产XXXX视频在线播放| 亚洲熟妇少妇任你躁在线观看无码| 欧美日韩免费在线视频| 欧美老妇交ZOZO| 无码日韩精品一区二区免费暖暖 | 97精品国产一区二区三区| 久久精品国产72国产精 | 人交獸AV完整版在线观看| 夜夜嗨AV一区二区三区| 一区二区国产精品精华| 东京热无码av男人的天堂| 日韩av有码中文字幕| 无码av无码天堂资源网z| 亚洲一区二区三区在线视频| WWW.色五月| 国产精品一级片一区二区| 性孕交大肚子孕妇| 黑人太大了太深了好痛 视频| 一性一交一口添一摸视频| 国产熟女肥臀精品国产馆乱|