TNNT3 rabbit pAb

TNNT3 rabbit pAb

AO-06-ES10399-50

TNNT3 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES10399
Product nameTNNT3 rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB;ELISA
Other name
Size50μL
Unit price ($)148
Human gene ID7140
Human Swiss-ProtP45378
SourceRabbit
IsotypeIgG
TargetTNNT3
Fields
Gene nameTNNT3
Protein nameTroponin T, fast skeletal muscle (TnTf) (Beta-TnTF) (Fast skeletal muscle troponin T) (fTnT)
Human gene link
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtQ9QZ47
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-ProtP09739
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from part region of human protein
SpecificityTNNT3 Polyclonal Antibody detects endogenous levels of protein.
FormulationLiquid in PBS containing 50% glycerol, and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000 ELISA 1:5000-20000
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)29kD
BackgroundThe binding of Ca(2+) to the trimeric troponin complex initiates the process of muscle contraction. Increased Ca(2+) concentrations produce a conformational change in the troponin complex that is transmitted to tropomyosin dimers situated along actin filaments. The altered conformation permits increased interaction between a myosin head and an actin filament which, ultimately, produces a muscle contraction. The troponin complex has protein subunits C, I, and T. Subunit C binds Ca(2+) and subunit I binds to actin and inhibits actin-myosin interaction. Subunit T binds the troponin complex to the tropomyosin complex and is also required for Ca(2+)-mediated activation of actomyosin ATPase activity. There are 3 different troponin T genes that encode tissue-specific isoforms of subunit T for fast skeletal-, slow skeletal-, and cardiac-muscle. This gene encodes fast skeletal troponin T protein; als
Functionalternative products:Additional isoforms seem to exist,disease:Defects in TNNT3 are a cause of distal arthrogryposis type 2B (DA2B) [MIM:601680]; also known as arthrogryposis multiplex congenita, distal, type 2B (AMCD2B). DA2B is a form of inherited multiple congenital contractures. Affected individuals have vertical talus, ulnar deviation in the hands, severe camptodactyly, and a distinctive face characterized by a triangular shape, prominent nasolabial folds, small mouth and a prominent chin.,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.,similarity:Belongs to the troponin T family.,tissue specificity:In fetal and adult fast skeletal muscles, with a higher level expression in fetal than in adult muscle.,
Subcellular locationcytosol,troponin complex,
ExpressionIn fetal and adult fast skeletal muscles, with a higher level expression in fetal than in adult muscle.

Additional Images

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Western blot analysis of lysates from SH-SY5Y cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES10399-50
: 10 Produits
Hurry! only 10 items left in stock.

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