精品国产av自拍_精品日韩欧美在线视频一区二区_一区二区在线观看在线_福利在线观看免费高清完整版_无码免费动漫老黄网站_无码一区在线观看视频_精品五月精品婷婷_免费国产日本高清_亚洲特黄特色一级在线观看_国产Ⅴ亚洲Ⅴ欧美Ⅴ专区

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  關(guān)于我們  聯(lián)系我們
91精品国自产在线观看,荡娃艳妇有声小说,亚洲欧美日韩在线视频
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-Cardiac Troponin T/Cy5 Conjugated antibody (bs-10648R-Cy5)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-10648R-Cy5
英文名稱 Rabbit Anti-Cardiac Troponin T/Cy5 Conjugated antibody
中文名稱 Cy5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(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 心血管  免疫學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Rat,  (predicted: Mouse, Dog, Pig, Cow, )
產(chǎn)品應(yīng)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(chǎn)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(quán)所有 2004-2026 0592123.cn 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
欧美日韩国产综合草草 | 娇喘嗯嗯~轻点啊视频福利 | 国产美女一级做a爱视频 | 老外和中国女人毛片免费视频 | AAAAA级少妇高潮大片免费 | **一级毛片全部免 | 内射一面膜上边一面膜下边 | 日韩精品免费在线观看 | 免费永久观看美女视频网站网址 | 免费可以看黄的视频s色 | www.xxxx黄色视频| 亚洲有码中文字幕一区 | 538精品A∨在线高清视频 | 2021无码天堂在线 | 成人女人a毛片在线看 | 日韩成人精品视频免费专区 | 亚洲精品欧美精品中文字幕 | 欧美日韩一区精品高免费专区 | 欧美精品亚洲精品日韩专区 | 午夜一区欧美二区高清三区 | 班长让我坐在那个地方教我作业 | 亚洲另类春色国产精品 | 久久精品中文字幕无码有码 | 亚洲日韩国产一区二区蜜桃 | 亚洲AV无码一二区三区在线播放 | 3d无尽的性人妖 | 欧美综合中文字幕久久99 | 国产Av人片乱码色午夜 | 国产成人综合亚洲欧美日韩 | 美国一级大黄一片免费的网站 | 在线观看国产精品第一区免费 | 午夜无码片在线观看影院 | 亚洲成AV人片一区二区三区 | 免费看撕开奶罩揉吮奶头视频 | 亚洲无人区码一二三码区别图片 | 91秦先生久久久久久久 | 夜夜高潮夜夜爽35高清视频 | 成年在线影视免费观看 | 伊人久久大香线蕉AV超碰 | 国产精品美女WWW爽爽爽视频 | 一区二区三区精品视频 |