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首頁(yè) > 抗體 > 一抗 > 其它 > Troponin I-C Monoclonal Antibody
Troponin I-C Monoclonal Antibody
商品貨號(hào)： PLA005070
適 應(yīng) 性： 人
WB IHC IF ELISA
￥600元
規(guī)格：
在線咨詢
MSDS
說(shuō)明書
商品描述
  • 發(fā)貨日期： 7
  • 基因名稱： TNNI3
  • 蛋白名稱： Troponin I cardiac muscle
  • Human_gene_id： 7137
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=7137
  • Human_swiss_prot_no： P19429
  • Human_swiss_link： http://www.uniprot.org/uniprotkb/P19429/entry
  • Mouse_swiss_prot_no： P48787
  • Mouse_swiss_link： http://www.uniprot.org/uniprot/P48787
  • 特異性： Troponin I-C Monoclonal Antibody detects endogenous levels of Troponin I-C protein.
  • 組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來(lái)源： Monoclonal, Mouse
  • 稀釋： WB 1:500 - 1:2000. IHC 1:200 - 1:1000. ELISA: 1:10000.. IF 1:50-200
  • 純化工藝： Affinity purification
  • 儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說(shuō)明書： 1
  • Msds： MSDS_Antibody.pdf
  • 其他名稱： TNNI3; TNNC1; Troponin I; cardiac muscle; Cardiac troponin I
  • 信號(hào)通路： Cardiac muscle contraction;Hypertrophic cardiomyopathy (HCM);Dilated cardiomyopathy;
  • 功能： disease:Defects in TNNI3 are the cause of cardiomyopathy dilated type 2A (CMD2A) [MIM:611880]. 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.,disease:Defects in TNNI3 are the cause of cardiomyopathy familial hypertrophic type 7 (CMH7) [MIM:191044]. 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.,disease:Defects in TNNI3 are the cause of cardiomyopathy familial restrictive type 1 (RCM1) [MIM:115210]. RCM1 is an heart muscle 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.,function:Troponin I is the inhibitory subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity.,similarity:Belongs to the troponin I family.,subunit:Binds to actin and tropomyosin. Interacts with TRIM63.,
  • 相關(guān)產(chǎn)品： YT4749,YT4748,YP0723,YP0321,KA1419C,KA1345C
  • 細(xì)胞定位： cytosol,troponin complex,sarcomere,
  • 組織表達(dá)： Heart,Heart muscle,PCR rescued clones,
  • 科研貨號(hào)： PLA005070
Troponin I-C Monoclonal Antibody
Catalog No PLA005070
Product information
  • 發(fā)貨日期： 7
  • 基因名稱： TNNI3
  • 蛋白名稱： Troponin I cardiac muscle
  • Human_gene_id： 7137
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=7137
  • Human_swiss_prot_no： P19429
  • Human_swiss_link： http://www.uniprot.org/uniprotkb/P19429/entry
  • Mouse_swiss_prot_no： P48787
  • Mouse_swiss_link： http://www.uniprot.org/uniprot/P48787
  • 特異性： Troponin I-C Monoclonal Antibody detects endogenous levels of Troponin I-C protein.
  • 組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來(lái)源： Monoclonal, Mouse
  • 稀釋： WB 1:500 - 1:2000. IHC 1:200 - 1:1000. ELISA: 1:10000.. IF 1:50-200
  • 純化工藝： Affinity purification
  • 儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說(shuō)明書： 1
  • Msds： MSDS_Antibody.pdf
  • 其他名稱： TNNI3; TNNC1; Troponin I; cardiac muscle; Cardiac troponin I
  • 信號(hào)通路： Cardiac muscle contraction;Hypertrophic cardiomyopathy (HCM);Dilated cardiomyopathy;
  • 功能： disease:Defects in TNNI3 are the cause of cardiomyopathy dilated type 2A (CMD2A) [MIM:611880]. 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.,disease:Defects in TNNI3 are the cause of cardiomyopathy familial hypertrophic type 7 (CMH7) [MIM:191044]. 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.,disease:Defects in TNNI3 are the cause of cardiomyopathy familial restrictive type 1 (RCM1) [MIM:115210]. RCM1 is an heart muscle 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.,function:Troponin I is the inhibitory subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity.,similarity:Belongs to the troponin I family.,subunit:Binds to actin and tropomyosin. Interacts with TRIM63.,
  • 相關(guān)產(chǎn)品： YT4749,YT4748,YP0723,YP0321,KA1419C,KA1345C
  • 細(xì)胞定位： cytosol,troponin complex,sarcomere,
  • 組織表達(dá)： Heart,Heart muscle,PCR rescued clones,
  • 科研貨號(hào)： PLA005070
    • Hunan UPT Biotechnology Co.,Ltd
    Website：www.jx3dscan.com Servive hotline :4006916686
    E-mail：service@uptbio.com
    Address：
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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