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
久热这里只有精品视频6,国产狂喷潮在线观看,精品久久8x国产免费观看
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Cardiac Troponin T/PE-Cy3 Conjugated antibody (bs-10648R-PE-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-10648R-PE-Cy3
英文名稱1 Rabbit Anti-Cardiac Troponin T/PE-Cy3 Conjugated antibody
中文名稱 PE-Cy3標記的心肌特異性肌鈣蛋白T抗體
別    名 Cardiac muscle troponin T; Cardiomyopathy dilated 1D (autosomal dominant); Cardiomyopathy hypertrophic 2; CMD1D; CMH2; CMPD2; cTnT; LVNC6; MGC3889; OTTHUMP00000033864; OTTHUMP00000033865; OTTHUMP00000033866; OTTHUMP00000033867; OTTHUMP00000033870; OTTHUMP00000218095; RCM3; TNNT 2; TNNT2; TNNT2_HUMAN; TnTC; Troponin T cardiac muscle; Troponin T type 2 (cardiac); Troponin T type 2 cardiac; Troponin T, cardiac muscle; Troponin T2; Troponin T2 cardiac.  
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  免疫學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, Rat,  (predicted: Mouse, Dog, Pig, Cow, )
產品應用 Flow-Cyt=1:50-200 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 36kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Cardiac Troponin T
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:
The protein encoded by this gene is the tropomyosin-binding subunit of the troponin complex, which is located on the thin filament of striated muscles and regulates muscle contraction in response to alterations in intracellular calcium ion concentration. Mutations in this gene have been associated with familial hypertrophic cardiomyopathy as well as with dilated cardiomyopathy. Transcripts for this gene undergo alternative splicing that results in many tissue-specific isoforms, however, the full-length nature of some of these variants has not yet been determined. [provided by RefSeq].

Function:
Troponin T is the tropomyosin-binding subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity.

Subcellular Location:
Cytoplasm.

Tissue Specificity:
Heart. The fetal heart shows a greater expression in the atrium than in the ventricle, while the adult heart shows a greater expression in the ventricle than in the atrium. Isoform 6 predominates in normal adult heart. Isoforms 1, 7 and 8 are expressed in fetal heart. Isoform 7 is also expressed in failing adult heart.

DISEASE:
Cardiomyopathy, familial hypertrophic 2 (CMH2) [MIM:115195]: 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. Note=The disease is caused by mutations affecting the gene represented in this entry.
Cardiomyopathy, dilated 1D (CMD1D) [MIM:601494]: A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. Note=The disease is caused by mutations affecting the gene represented in this entry.
Cardiomyopathy, familial restrictive 3 (RCM3) [MIM:612422]: A heart disorder characterized by impaired filling of the ventricles with reduced diastolic volume, in the presence of normal or near normal wall thickness and systolic function. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the troponin T family.

Database links:

Entrez Gene: 493940 Cat

Entrez Gene: 286816 Cow

Entrez Gene: 403532 Dog

Entrez Gene: 7139 Human

Entrez Gene: 21956 Mouse

Entrez Gene: 100622450 Pig

Entrez Gene: 100009428 Rabbit

Entrez Gene: 24837 Rat

Omim: 191045 Human

SwissProt: P13789 Cow

SwissProt: P45379 Human

SwissProt: P50752 Mouse

SwissProt: P09741 Rabbit

SwissProt: P50753 Rat

Unigene: 533613 Human

Unigene: 247470 Mouse

Unigene: 9965 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: 国产亚洲一区二区在线观看99| 毛色av一区二区| 国产色在线观看AV| 成年女子黄网站18禁绯:色AV| 91精品国产91久久久久青草 | 香蕉视频免费下载安装软件 | 在线播放免费毛片r有呵呵蜜桃传说 | 888亚洲欧美国无码精品| 亚洲欧洲精品一区二区三区软件| 天堂8在线天堂资源在线,美丽姑娘在线观看完整版中文 | 波多野结衣中文在线播放1区2区| 一区二区不卡视频在线观看| 日韩蜜芽精品视频在线观看网站| 激情小说 在线视频 3d| 最新日韩无人在线AV| 中国精品男Gay片爽免费| 无码日韩人妻精品久久蜜桃免费天天| 久久久久亚洲精品无码网址,久久久久亚洲| 国产女主播在线观看手机免费| 伊人中出手机在线| 蜜臀98精品国产免费观看,女教师高潮| 国产成人精品一区二区三区免费无码高清不卡| 尤物youwu193视频播放| 久久亚洲春色中文字幕久久久... 久久亚洲国产成人精品无码区 亚洲AV无 | 亚洲精品国产无套在线观 | 草莓视频做爰视频免费观看| 新久久久久久一级毛片免费看| 狠狠色狠狠色综合日日不卡卡| 一级毛片免费完整视频初女 | 伊人久久精品亚洲午夜,久久99精品 | 黑人英雄爱吃土豆西红柿口诀| 中文字幕第30页一区二区| 里番ACG里番本子全彩软件测评无毒不卡| 国产丝袜调教视频足j| 亚州熟妇Av影视| 成人免a亚洲在| 日韩精品一区二三区中文-亚洲高清偷拍一区二区三区 | 97精品一区二区视频在线观看 | 欧美操B操B操、B| 91蝌蚪在线播放白丝| 久久夜色精品国产噜噜亚洲AV_天天 |