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NSJ Bioreagents

SKU:RQ4616

Cardiac Troponin T Antibody / CTnT / TNNT2

Cardiac Troponin T Antibody / CTnT / TNNT2

Regular price $449.00 USD
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Cardiac muscle troponin T (cTnT), is a protein which in humans is encoded by the TNNT2 gene. It is mapped to 1q32.1. 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.

Specifications

Family Primary antibody
Formulation 0.5mg/ml if reconstituted with 0.2ml sterile DI water
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit IgG
Species Reactivity Mouse, Rat
Application WB, Direct ELISA
Application Details Western blot: 0.5-1ug/ml,Direct ELISA: 0.1-0.5ug/ml
Application Note Optimal dilution of the Cardiac Troponin T antibody should be determined by the researcher.
Immunogen Amino acids K88-K298 from the human protein were used as the immunogen for the Cardiac Troponin T antibody.
Buffer Lyophilized from 1X PBS with 2% Trehalose and 0.025% sodium azide
Purity Antigen affinity purified
Storage After reconstitution, the Cardiac Troponin T antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
Uniprot # P45379
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/cardiac-troponin-t-antibody-ctnt-tnnt2-rq4616
Title Cardiac Troponin T Antibody / CTnT / TNNT2
Description Cardiac muscle troponin T (cTnT), is a protein which in humans is encoded by the TNNT2 gene. It is mapped to 1q32.1. 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.
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