Product Name
Cardiac Troponin-I (TNNI3), Recombinant Protein
Popular Item
Full Product Name
Recombinant Human Cardiac Troponin-I, His Tag
Product Synonym Names
TNNI3 Human, His; Cardiac Troponin-I Human Recombinant, His Tag; Troponin I cardiac muscle; Cardiac troponin I; TNNI3; TNNC1; CMH7; RCM1; cTnI; CMD2A; MGC116817
Product Gene Name
TNNI3 recombinant protein
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for P19429
Purity/Purification
Protein is >95% pure as determined by 12% PAGE (coomassie staining).
Form/Format
TNNI3 protein solution (0.34 mg/mL) in PBS and 25 mM arginine.
Physical Appearance
Sterile Filtered Clear Solution.
Preparation and Storage
TNNI3 although stable at 4°C for 1 week , should be stored below -18°C. Please prevent freeze thaw cycles.
Other Notes
Small volumes of TNNI3 recombinant protein vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
TNNI3 recombinant protein
Introduction: Troponin I (TnI), troponin T (TnT) and troponin C (TnC) form the troponin complex of the thin filaments of striated muscle. TnI is acts as the inhibitory subunit by blocking actin-myosin interactions and thereby mediating striated muscle relaxation. The TnI subfamily contains 3 genes: TnI-skeletal-fast-twitch, TnI-skeletal-slow-twitch, and TnI-cardiac. The TNNI3 gene encodes the TnI-cardiac protein and is exclusively expressed in cardiac muscle tissues. Mutations in the TNNI3 gene cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM).
Description: Recombinant Human TNNI3 protein produced in E Coli is a full length protein containing a total of 260 amino acids and fused to a 6 His Tag at C-terminus, migrating as a 27kDa band on SDS-PAGE.
Purified by proprietary chromatographic technique.
Product Categories/Family for TNNI3 recombinant protein
RECOMBINANT & NATURAL PROTEINS
NCBI/Uniprot data below describe general gene information for TNNI3. It may not necessarily be applicable to this product.
NCBI Accession #
NP_000354.4
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NCBI GenBank Nucleotide #
NM_000363.4
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UniProt Primary Accession #
P19429
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UniProt Related Accession #
P19429[Other Products]
NCBI Official Full Name
troponin I, cardiac muscle
NCBI Official Synonym Full Names
troponin I3, cardiac type
NCBI Official Symbol
TNNI3??[Similar Products]
NCBI Official Synonym Symbols
CMH7; RCM1; cTnI; CMD2A; TNNC1; CMD1FF
??[Similar Products]
NCBI Protein Information
troponin I, cardiac muscle
UniProt Protein Name
Troponin I, cardiac muscle
UniProt Synonym Protein Names
Cardiac troponin I
UniProt Gene Name
TNNI3??[Similar Products]
UniProt Synonym Gene Names
TNNC1??[Similar Products]
UniProt Entry Name
TNNI3_HUMAN
UniProt Comments for TNNI3
TNNI3: Troponin I is the inhibitory subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity. Binds to actin and tropomyosin. Interacts with TRIM63. Interacts with STK4/MST1. Belongs to the troponin I family.
Protein type: Actin-binding; Motility/polarity/chemotaxis; Motor
Chromosomal Location of Human Ortholog: 19q13.4
Cellular Component: cytosol; sarcomere; troponin complex
Molecular Function: actin binding; calcium channel inhibitor activity; calcium-dependent protein binding; protein binding; protein domain specific binding; protein kinase binding; troponin C binding; troponin T binding
Biological Process: cardiac muscle contraction; cellular calcium ion homeostasis; heart contraction; heart development; muscle filament sliding; negative regulation of ATPase activity; regulation of systemic arterial blood pressure by ischemic conditions; skeletal muscle contraction; vasculogenesis; ventricular cardiac muscle morphogenesis
Disease: Cardiomyopathy, Dilated, 1ff; Cardiomyopathy, Dilated, 2a; Cardiomyopathy, Familial Hypertrophic, 7; Cardiomyopathy, Familial Restrictive, 1
Precautions
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Disclaimer
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