Protein name:
Troponin T, cardiac muscle (TnTc) ;
Alternative:
Cardiac muscle troponin T (cTnT) ;
Organism:
Human (Homo sapiens).
General Annotation
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:
N/A
Protein Attributes:
50:
MSDIEEVVEE | YEEEEQEEAA | VEEEEDWRED | EDEQEEAAEE | DAEAEAETEE |
100:
TRAEEDEEEE | EAKEAEDGPM | EESKPKPRSF | MPNLVPPKIP | DGERVDFDDI |
150:
HRKRMEKDLN | ELQALIEAHF | ENRKKEEEEL | VSLKDRIERR | RAERAEQQRI |
200:
RNEREKERQN | RLAEERARRE | EEENRRKAED | EARKKKALSN | MMHFGGYIQK |
250:
QAQTERKSGK | RQTEREKKKK | ILAERRKVLA | IDHLNEDQLR | EKAKELWQSI |
298:
YNLEAEKFDL | QEKFKQQKYE | INVLRNRIND | NQKVSKTRGK | AKVTGRWK
Vaild Sequence:
Related Databases
Uniprot:
ELISA Kit
CLIA Kit
Polyclonal Antibody
Monoclonal Antibody
Protein
FOR
Human
Mouse
Rat
Rabbit
Bovine
Chicken
Polyclonal Antibody for Human TnTc
Polyclonal Antibody for Human TnTc
Polyclonal Antibody for Human TnTc
Polyclonal Antibody for Human TnTc
Polyclonal Antibody for Human TnTc
Polyclonal Antibody for Human TnTc
Monoclonal Antibody for Human TnTc
Monoclonal Antibody for Human TnTc
Monoclonal Antibody for Human TnTc
Monoclonal Antibody for Human TnTc
Monoclonal Antibody for Human TnTc
Monoclonal Antibody for Human TnTc
R&D Technical Data
12% SDS-PAGE analysis
Western blot - Anti-TNNT2 antibody
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Precision
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Recovery
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Linearity
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References
1.
[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 6)
tissue :
Heart .
2.
[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 1; 6 AND 12)
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[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
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[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
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[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
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Fetal heart .
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[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : NUCLEOTIDE SEQUENCE [GENOMIC DNA] (ISOFORM 6);VARIANT CMH2 ILE-120
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Heart muscle .
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[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 6)
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Heart .
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[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]
11.
[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 11)
tissue :
Uterus .
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,
Schwartz K.
J. Mol. Cell. Cardiol.30:1247-1253(1998)
[
PubMed ]
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Europe PMC ]
[
Abstract ]
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Cited for : NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 191-229 AND 231-288;ALTERNATIVE SPLICING;VARIANT ARG-263
tissue :
Blood .
13.
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Cited for : PROTEIN SEQUENCE OF 70-76 AND 177-182
tissue :
Heart .
14.
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Cited for : X-RAY CRYSTALLOGRAPHY (2.61 ANGSTROMS) OF 193-298
15.
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Cited for : VARIANTS CMH2 ASN-89 AND GLN-102
16.
"Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy."
Watkins H.
,
McKenna W.J.
,
Thierfelder L.
,
Suk H.J.
,
Anan R.
,
O'Donoghue A.
,
Spirito P.
,
Matsumori A.
,
Moravec C.S.
,
Seidman J.G.
,
Seidman C.E.
N. Engl. J. Med.332:1058-1064(1995)
[
PubMed ]
[
Europe PMC ]
[
Abstract ]
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Cited for : VARIANTS CMH2 ILE-120; LYS-173; ASP-254 AND CYS-288
17.
"Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy."
Forissier J.F.
,
Carrier L.
,
Farza H.
,
Bonne G.
,
Bercovici J.
,
Richard P.
,
Hainque B.
,
Townsend P.J.
,
Yacoub M.H.
,
Faure S.
,
Dubourg O.
,
Millaire A.
,
Hagege A.A.
,
Desnos M.
,
Komajda M.
,
Schwartz K.
Circulation94:3069-3073(1996)
[
PubMed ]
[
Europe PMC ]
[
Abstract ]
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Cited for : VARIANT CMH2 LEU-102
18.
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Cited for : VARIANT CMH2 TRP-102
19.
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Cited for : VARIANT CMH2 PRO-288
20.
[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : VARIANT CMH2 LEU-104
21.
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Cited for : VARIANT CMH2 VAL-114
22.
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Cited for : VARIANT CMH2 PHE-189
23.
"Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy."
Kamisago M.
,
Sharma S.D.
,
DePalma S.R.
,
Solomon S.
,
Sharma P.
,
McDonough B.
,
Smoot L.
,
Mullen M.P.
,
Woolf P.K.
,
Wigle E.D.
,
Seidman J.G.
,
Seidman C.E.
N. Engl. J. Med.343:1688-1696(2000)
[
PubMed ]
[
Europe PMC ]
[
Abstract ]
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Cited for : VARIANT CMD1D LYS-210 DEL
24.
"Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy."
Li D.
,
Czernuszewicz G.Z.
,
Gonzalez O.
,
Tapscott T.
,
Karibe A.
,
Durand J.B.
,
Brugada R.
,
Hill R.
,
Gregoritch J.M.
,
Anderson J.L.
,
Quinones M.
,
Bachinski L.L.
,
Roberts R.
Circulation104:2188-2193(2001)
[
PubMed ]
[
Europe PMC ]
[
Abstract ]
[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : VARIANT CMD1D TRP-151
25.
"Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy."
Richard P.
,
Charron P.
,
Carrier L.
,
Ledeuil C.
,
Cheav T.
,
Pichereau C.
,
Benaiche A.
,
Isnard R.
,
Dubourg O.
,
Burban M.
,
Gueffet J.-P.
,
Millaire A.
,
Desnos M.
,
Schwartz K.
,
Hainque B.
,
Komajda M.
Circulation107:2227-2232(2003)
[
PubMed ]
[
Europe PMC ]
[
Abstract ]
[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : VARIANTS CMH2 LEU-80; VAL-120; ILE-281 AND CYS-296
26.
Richard P.
,
Charron P.
,
Carrier L.
,
Ledeuil C.
,
Cheav T.
,
Pichereau C.
,
Benaiche A.
,
Isnard R.
,
Dubourg O.
,
Burban M.
,
Gueffet J.-P.
,
Millaire A.
,
Desnos M.
,
Schwartz K.
,
Hainque B.
,
Komajda M.
Circulation109:3258-3258(2004)
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Cited for : ERRATUM
27.
"Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy."
Erdmann J.
,
Daehmlow S.
,
Wischke S.
,
Senyuva M.
,
Werner U.
,
Raible J.
,
Tanis N.
,
Dyachenko S.
,
Hummel M.
,
Hetzer R.
,
Regitz-Zagrosek V.
Clin. Genet.64:339-349(2003)
[
PubMed ]
[
Europe PMC ]
[
Abstract ]
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Cited for : VARIANT CMH2 PRO-288
28.
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Cited for : VARIANTS CMD1D TRP-141; LEU-215 AND LYS-220 DEL
29.
"Mutations profile in Chinese patients with hypertrophic cardiomyopathy."
Song L.
,
Zou Y.
,
Wang J.
,
Wang Z.
,
Zhen Y.
,
Lou K.
,
Zhang Q.
,
Wang X.
,
Wang H.
,
Li J.
,
Hui R.
Clin. Chim. Acta351:209-216(2005)
[
PubMed ]
[
Europe PMC ]
[
Abstract ]
[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : VARIANT CMH2 CYS-140
30.
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Cited for : VARIANT CMD1D TRP-151
31.
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Cited for : VARIANT CMH2 CYS-288
32.
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Cited for : INVOLVEMENT IN RCM3
33.
"Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy."
Millat G.
,
Bouvagnet P.
,
Chevalier P.
,
Sebbag L.
,
Dulac A.
,
Dauphin C.
,
Jouk P.S.
,
Delrue M.A.
,
Thambo J.B.
,
Le Metayer P.
,
Seronde M.F.
,
Faivre L.
,
Eicher J.C.
,
Rousson R.
Eur. J. Med. Genet.54:E570-E575(2011)
[
PubMed ]
[
Europe PMC ]
[
Abstract ]
[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : VARIANTS CMH2 VAL-38 AND CYS-288;VARIANTS CMD1D TRP-141 AND LYS-220 DEL