亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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
99久久人妻精品免费一区,99国产精品无码,性色av无码中文av有码vr
Rabbit Anti-Tropomyosin/RBITC Conjugated antibody (bs-9622R-RBITC)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@www.chomd.com.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@www.chomd.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-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(shū) 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.www.chomd.com.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)
主站蜘蛛池模板: 精品无人区麻豆乱码1区2区新区_精品日产 | 3D精品重口另类爱| 中文字幕精品一区二区精品电影| 亚洲一本一道最新地址| 久热re6只有视频精品| 成人黄色在线网站观看污| 亚洲午夜成激人情在线影院免费观看| 人妻熟妇中文字幕完整版| 国产成人久久精品激情日韩电影免费 | 亚洲h在线播放在线观看H| 久久亚洲AV日韩AV无码A| 大蟒蛇jakeandrich视频可播放| 亚洲天码不卡熟女| 激情综合婷婷丁香五月可下载| 在线天堂中文在线资源网8在线中文| 人人妻人人澡人人爽人人精品97_亚洲一 | 新版天堂8资源在线下载安装 | 午夜精品久久久久久中宇,亚洲一区二区三区无码国产 | 三级国产网站养生女spa| 丰满少妇作爱视频免费观看夫妻隔帘按摩视频 | 中午字幕在线观看视频2019| 人人妻人人爽人人澡人人免费 | 成人乱视频网站能看| 色欲一区二区三区| GAY片男同网站www免费| 人人妻人人澡人人爽国产一区 | 激情97综合亚洲色婷婷五,国产JK白丝喷白浆在线... | 久久大香伊蕉在人线国产H_女人高潮抽| a毛片毛片看免费免费| 人人爽人人爽人人片AV - 国产精| 97久久精品人妻人人搡人人玩,99国内 | 国产99久久久国产精品成人免费 | cum4k国产精品偷自区| 女人抽搐喷水高潮国产精品| 中文字幕中文字幕中文字幕中文字幕夜夜双头龙| 色婷婷狠狠五月综合舔| 中文字幕无码综合在线管看| 久久国产成人精品护士| 亚洲爆乳少妇无码激情小说| a级毛片无码视频AAAA流出91 | 无码专区久久综合久中文字幕乱|