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
日韩内射美女人妻一区二区三区 ,精品国产污污免费网站入口 ,人妻丰满熟妇AV无码区APP
Rabbit Anti-Tropomyosin/RBITC Conjugated antibody (bs-9622R-RBITC)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@xucheq.com
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說(shuō) 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-9622R-RBITC
英文名稱1 Rabbit Anti-Tropomyosin/RBITC Conjugated antibody
中文名稱 羅丹明(RBITC)標(biāo)記的原肌球蛋白1抗體
別    名 Tropomyosin 1 (alpha); Alpha tropomyosin; Alpha-tropomyosin; C15orf13; cardiomyopathy, hypertrophic 3; CMD1Y; CMH3; HTM alpha; sarcomeric tropomyosin kappa; TMSA; TPM1; TPM1_HUMAN; Tropomyosin 1; Tropomyosin1; Tropomyosin alpha 1 chain; Tropomyosin alpha-1 chain; Tropomyosin-1; Tropomyosin α; Tropomyosin-α; Tropomyosinα.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說(shuō) 明 書 100ul  
研究領(lǐng)域 心血管  信號(hào)轉(zhuǎn)導(dǎo)  細(xì)胞骨架  細(xì)胞外基質(zhì)  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human,  (predicted: Mouse, Rat, Dog, Zebrafish, Sheep, )
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 Tropomyosin
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:
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.

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.

Subunit:
Heterodimer of an alpha and a beta chain (By similarity). Interacts with HRG (via the HRR domain); the interaction contributes to the antiangiogenic properties of the histidine/proline-rich region (HRR) of HRG.

Subcellular Location:
Cytoplasm, cytoskeleton.

Tissue Specificity:
Detected in primary breast cancer tissues but undetectable in normal breast tissues in Sudanese patients. Isoform 1 is expressed in adult and fetal skeletal muscle and cardiac tissues, with higher expression levels in the cardiac tissues. Isoform 10 is expressed in adult and fetal cardiac tissues, but not in skeletal muscle.

Post-translational modifications:
Phosphorylated at Ser-283 by DAPK1 in response to oxidative stress and this phosphorylation enhances stress fiber formation in endothelial cells.

DISEASE:
Defects in TPM1 are the cause of familial hypertrophic cardiomyopathy type 3 (CMH3) [MIM:115196]. Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.
Defects in TPM1 are the cause of cardiomyopathy dilated type 1Y (CMD1Y) [MIM:611878]. Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.

Similarity:
Belongs to the tropomyosin family.

Database links:

Entrez Gene: 7168 Human

Entrez Gene: 22003 Mouse

Entrez Gene: 100037999 Pig

Entrez Gene: 24851 Rat

Entrez Gene: 30324 Zebrafish

Omim: 191010 Human

SwissProt: Q5KR49 Cow

SwissProt: P09493 Human

SwissProt: P58771 Mouse

SwissProt: P42639 Pig

SwissProt: P04692 Rat

SwissProt: P13104 Zebrafish

Unigene: 133892 Human

Unigene: 121878 Mouse

Unigene: 87540 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(guò)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(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
无码视频一区二区三区| 日本护士毛茸茸| 久久夜色精品国产噜噜亚洲av| 国产一区二区三区| 男人的好免费观看直播| 黑人大荫道BBWBBB高潮潮喷| 精品国产一区二区三区久久| 18禁高潮出水呻吟娇喘蜜芽| 精品国产成人亚洲午夜福利| 99久久无码一区人妻A片竹菊| 好色先生下载| 日本LAURENPHILIPS| 久久精品A亚洲国产V高清不卡| 亚洲色偷精品一区二区三区| 国产麻豆精品一区二区三区| 日韩久久无码免费毛片软件| 日韩精品无码一本二本三本色 | 国产精品无码专区| 国产男女猛烈无遮挡免费视频网站| 亚洲日本无码一区二区三区四区卡| 亚洲AV无码成人精品区在线观看| 国产精品亚洲ΑV天堂无码| 国产国语老龄妇女a片| 国产,日韩,丝袜,欧美一区| 精品久久久久久无码国产| 无码人妻精品中文字幕| 97人妻精品一区二区三区| 亚洲熟妇AV一区二区三区漫画| 岳把我用嘴含进满足我视频| 麻豆亚洲AV成人无码久久精品| АⅤ资源天堂资源库在线| 久久九九久精品国产免费直播 | 亚洲精品婷婷无码成人A片在线| 久久青青草原亚洲AV无码麻豆 | 无码AV中文字幕久久专区| 无码AV免费一区二区三区试看| 日本亲近相奷中文字幕| 日韩精品久久无码中文字幕| 久久国产精品波多野结衣AV| 国偷自产AV一区二区三区| 老熟女HDXX老小配|