超碰97自拍_久久99久久98精品免观看软件_在线亚洲一区_九九视频这里只有精品_国产精品一区二区欧美视频_精品国产区一区

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  關于我們  聯系我們
99久久夜色精品,av色综合久久天堂av色综合,国产免费一级一级
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Cardiac Troponin T/PE-Cy5.5 Conjugated antibody (bs-10648R-PE-Cy5.5)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-10648R-PE-Cy5.5
英文名稱 Rabbit Anti-Cardiac Troponin T/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5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.ggggww.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: 日韩午夜激情 | 裸体美女扒开下部无遮挡网站免费 | 久久综合色网 | 无码AⅤ免费中文字幕久久 日韩福利一区 | 日韩美女视频在线观看 | 久久99热这里只频精品6 | 999在线观看视频 | 亚洲免费观看网站 | 国产香蕉97碰碰久久人人九色 | 九九精品视频在线观看 | 日本公妇乱淫免费视频一区三区 | 扒开双腿疯狂进出爽爽爽动态图 | 91精品久久久久五月天精品 | 欧美aaa一级片 | 亚洲激情成人网 | 人成久久 | 最新精品视频2020在线视频 | 中国老太老妇xx对白 | 亚洲一区二区三区尿失禁 | 国产一区二区三区美女 | 国产成人精品久久久一区二区三区 | 国产一级片每日更新 | 超薄肉色丝袜一二三四区 | 亚洲精品久久无码AV片银杏 | 亚洲乱码国产乱码精品精的特点 | 铠甲勇士第一部52集全 | 99久久免费看精品国产一区非洲 | 无遮挡十八禁污污网站免费 | 黄色高清免费 | 26uuu成人| 免费一对一刺激互动聊天软件 | JK小仙女自慰流白浆呻吟 | 拍真实国产伦偷精品 | 国产在线观看免费av | 亚洲av色欲色欲www | 99精品人妻少妇一区二区 | 在线观看AV片永久免费 | 亚欧美无遮挡HD高清在线视频 | 无码国产精品一区二区免费虚拟VR | 亚洲色成人一区二区三区小说 | 一区二区三区观看 |