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    Cardiac Troponin I/TNNC1 Recombinant Rabbit mAb (bsm-52818R)  
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    產(chǎn)品編號 bsm-52818R
    英文名稱(chēng) Cardiac Troponin I/TNNC1 Recombinant Rabbit mAb
    中文名稱(chēng) 心肌肌鈣蛋白重組兔單抗
    別    名 TNNC1; Troponin I; cardiac muscle; Cardiac troponin I; TNNI3; CMD2A.  
    抗體來(lái)源 Rabbit
    克隆類(lèi)型 Recombinant
    克 隆 號 6G15
    交叉反應 Human
    產(chǎn)品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:50-200,IP=1:20-50
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 24 kDa
    檢測分子量
    細胞定位 細胞漿 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 A synthesized peptide derived from human Troponin I: 1-48 
    亞    型 IgG
    純化方法 affinity purified by Protein A
    緩 沖 液 10mM phosphate buffered saline(pH 7.4) with 150mM sodium chloride, 0.05% BSA, 0.02% Proclin300 and 50% glycerol.
    保存條件 Store at 4℃ for short term. Store at -20℃ for long term. Avoid repeated freeze/thaw cycles.
    注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    PubMed PubMed
    產(chǎn)品介紹 Troponin I (TnI), along with troponin T (TnT) and troponin C (TnC), is one of 3 subunits that form the troponin complex of the thin filaments of striated muscle. TnI is the inhibitory subunit; blocking actin-myosin interactions and thereby mediating striated muscle relaxation. The TnI subfamily contains three genes: TnI-skeletal-fast-twitch, TnI-skeletal-slow-twitch, and TnI-cardiac. This gene encodes the TnI-cardiac protein and is exclusively expressed in cardiac muscle tissues. Mutations in this gene cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM). [provided by RefSeq, Jul 2008]

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

    Subunit:
    Binds to actin and tropomyosin. Interacts with TRIM63. Interacts with STK4/MST1.

    Post-translational modifications:
    Phosphorylated at Ser-42 and Ser-44 by PRKCE; phosphorylation increases myocardium contractile dysfunction. Phosphorylated at Ser-23 and Ser-24 by PRKD1; phosphorylation reduces myofilament calcium sensitivity. Phosphorylated preferentially at Thr-31. Phosphorylation by STK4/MST1 alters its binding affinity to TNNC1 (cardiac Tn-C) and TNNT2 (cardiac Tn-T).

    DISEASE:
    Defects in TNNI3 are the cause of familial hypertrophic cardiomyopathy type 7 (CMH7) [MIM:613690]. 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. Defects in TNNI3 are the cause of familial restrictive cardiomyopathy type 1 (RCM1) [MIM:115210]. RCM1 is a 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. 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. Defects in TNNI3 are the cause of cardiomyopathy dilated type 1FF (CMD1FF) [MIM:613286]. 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.

    Similarity:
    Belongs to the troponin I family.

    SWISS:
    P19429

    Gene ID:
    7137

    Database links:

    Entrez Gene : 7137 Human

    Entrez Gene : 21954 Mouse

    Entrez Gene : 100049696 Pig

    Entrez Gene : 29248 Rat

    Omim : 191044 Human

    SwissProt : P19429 Human

    SwissProt : P48787 Mouse

    SwissProt : P23693 Rat

    Unigene : 709179 Human

    Unigene : 27674 Mouse

    Unigene : 64141 Rat



    心肌肌鈣蛋白(Cardiac Troponin CTn1)是心肌收縮的調節蛋白,存在于心肌收縮蛋白的細肌絲上。肌鈣蛋白的作用之一是把原肌凝蛋白(Tropomyosin.Tm)附著(zhù)于肌動(dòng)蛋白(Action.A)上、 主要用于心肌功能方面的研究。
    產(chǎn)品圖片
    Western blot analysis of fetal heart cell lysate. Using Cardiac Troponin I/TNNC1 (bsm-52818R) monoclonal antibody at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at r.t. for 60 min.
    Paraformaldehyde-fixed, paraffin embedded Human Heart; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; Antibody incubation with Cardiac Troponin I/TNNC1 Monoclonal Antibody, Unconjugated(bsm-52818R) at 1:200 overnight at 4°C, followed by conjugation to the bs-0295G-HRP and DAB (C-0010) staining and DAB (C-0010) staining.
    (Negative control) Paraformaldehyde-fixed, paraffin embedded Human Cerebrum; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; Antibody incubation with Cardiac Troponin I/TNNC1 Monoclonal Antibody, Unconjugated(bsm-52818R) at 1:200 overnight at 4°C, followed by conjugation to the bs-0295G-HRP and DAB (C-0010) staining and DAB (C-0010) staining.
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