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

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  人才招聘  關于我們  聯系我們
欧美videosdesexo肥婆,亚洲videosbestsex日本,国产免费一区二区三区免费视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Tropomyosin/Cy3 Conjugated antibody (bs-9622R-Cy3)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-9622R-Cy3
英文名稱1 Rabbit Anti-Tropomyosin/Cy3 Conjugated antibody
中文名稱 Cy3標記的原肌球蛋白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.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 心血管  信號轉導  細胞骨架  細胞外基質  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,  (predicted: Mouse, Rat, Dog, Zebrafish, Sheep, )
產品應用 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 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.
版權所有 2004-2026 www.www.chomd.com.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 丝袜美腿美女一区二区动态| 久久一区二区精品直播| 国产精品.日产无码51| 最新中文字幕视频日韩视频中文字幕视频在线观看 | 一区二区三区911播放| 日韩人妻无码一区二区三区99噢美 | 亚洲精品无码人妻无码..,亚洲精品国| 色综合天天综合狠狠爱亚洲色视频| 精品久久久久中文字|欧美VA日韩VA人妻VA|久久| 国产三级A三级三级Gif动态图 | 91精品国产自产91精品资源,色综合久| 亚洲国产精品无码久久久蜜芽小说| 久久一区二区三区精品无 | 久久久久久亚洲精品不卡无码| heyzo在线播放中文av| 三上悠亚 亚洲一区二区三区 在线 | 精品无码一区二区三区亚洲桃色_| 97久久久久亚洲vA无码区首页 | 久久久久久人妻无码3D| 2019香蕉在线观看直播视频下载| 无码国内精品人妻少妇在小视频 | 久久久久亚洲AV无码六十路老熟| 91精品国产色综合久久不8男同| 日日狠狠久久偷偷色综合昆山| 国产成人无码18禁午夜福利p时刻 国产成人无码18禁午夜福利网址木青 | 久久久久久亚洲精品不卡无码 | 国内国外日产一区二区免费完整版| 亚洲字幕在线观看极品| 精品久久久久久国产91边打电话边后入 | 中文字幕亚洲一区二区三区视频网 | 隔着薄薄的肉色丝袜进入她的身体 | 天堂8在线天堂资源在线,美丽姑娘在线观看完整版中文 | 一本一道人人妻人人妻a| 精品一区二区三区中文字幕在线观看污污| 中文字幕日韩一区二区不卡人妻电影| 男人的天堂一区二区三区日韩| 18禁男女爽爽爽午夜网站免费有码 | 国产97在线观看观看| 欧美无砖专区在线播放| 永久亚洲成a人片777777 午夜福利 | 亚洲一区二区三区久久久久久国产99 |