心肌特异性肌钙蛋白罢抗体
规格：1尘驳/1尘濒
英文名： Cardiac Troponin T
别名： Cardiac muscle troponin T; Cardiomyopathy dilated 1D (autosomal dominant); Cardiomyopathy hypertrophic 2; CMD1D; CMH2; CMPD2; cTnT; LVNC6; MGC3889; OTTHUMP00000033864; OTTHUMP00000033865; OTTHUMP00000
分子量： 36kDa
储存液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce
克隆类型：笔辞濒测肠濒辞苍补濒
亚型：滨驳骋
纯化方法：affinity purified by Protein A
**原：KLH conjugated synthetic peptide derived from human Cardiac
交叉反应：Human, Mouse, Rat, Dog, Pig, Cow,
细胞定位：细胞浆
心肌特异性肌钙蛋白罢抗体产物介绍：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 heart shows a greater expression in the ventricle than in the atrium. Isoform 6 predominates in normal heart. Isoforms 1, 7 and 8 are expressed in fetal heart. Isoform 7 is also 心肌特异性肌钙蛋白罢抗体expressed in failing 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心肌特异性肌钙蛋白罢抗体 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. Gene ID: 7139 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.
心肌特异性肌钙蛋白罢抗体产物应用：WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1:20-200 ICC=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
研究领域：心血管 **学
储存条件： Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
来源： Rabbit
外观： Lyophilized or Liquid