TNNT1 antibody - middle region

Katalog-Nummer ARP42120_P050

Size : 100ul

Marke : Aviva Systems Biology

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TNNT1 Antibody - middle region (ARP42120_P050)

Datasheets/ManualsPrintable datasheet for anti-TNNT1 (ARP42120_P050) antibody
Product Info
Tested Species ReactivityHuman, Mouse
Predicted Species ReactivityHuman, Mouse, Rat, Cow, Dog, Guinea Pig, Horse, Zebrafish
Product FormatLiquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
ClonalityPolyclonal
HostRabbit
ApplicationWB
Reconstitution and StorageFor short term use, store at 2-8C up to 1 week. For long term storage, store at -20C in small aliquots to prevent freeze-thaw cycles.
ImmunogenThe immunogen is a synthetic peptide directed towards the middle region of human TNNT1
PurificationAffinity Purified
Predicted Homology Based on Immunogen SequenceCow: 100%; Dog: 100%; Guinea Pig: 100%; Horse: 100%; Human: 100%; Mouse: 100%; Rat: 100%; Zebrafish: 85%
Peptide SequenceSynthetic peptide located within the following region: WIHQLESEKFDLMAKLKQQKYEINVLYNRISHAQKFRKGAGKGRVGGRWK
Concentration0.5 mg/ml
Blocking PeptideFor anti-TNNT1 (ARP42120_P050) antibody is Catalog # AAP42120 (Previous Catalog # AAPP24505)
Enhanced Validation
WBY
SPR
YCHAROS
ReferenceWitt,S.H., (2005) J. Mol. Biol. 350 (4), 713-722
Gene SymbolTNNT1
Gene Full NameTroponin T type 1 (skeletal, slow)
Alias SymbolsANM, TNT, NEM5, STNT, TNTS
NCBI Gene Id7138
Protein NameTroponin T, slow skeletal muscle
Description of TargetTNNT1 is a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year.This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene.
Uniprot IDP13805
Protein Accession #NP_003274
Nucleotide Accession #NM_003283
Protein Size (# AA)278
Molecular Weight33kDa
Protein InteractionsCCDC136; TFIP11; LDOC1; MORF4L1; TBPL1; TPM3; TPM1; TNNT1; NFE2L2; KRT40; UBC; PI4KA; SERPINA4; OSM; MARS; HSP90AB1; FYN; EEF1G; DDX5; CHD3; BLOC1S2; C2orf44; ZNF768; ZNF250; ZC3H15; NAGK; HMP19; TRA2A; TMEM98; ARMC8; OSBP2; ZKSCAN5; LARP1; NACAD; SNW1; S

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