TNNT3 anticorps (AA 45-251)

N° du produit ABIN7601762

Cet anticorps anti-TNNT3 est un anticorps Lapin Polyclonal détectant TNNT3 dans WB et ELISA. Adapté pour Humain, Souris et Rat.

Aperçu rapide pour TNNT3 anticorps (AA 45-251) (ABIN7601762)

Antigène: TNNT3 (Fast Skeletal Troponin T (TNNT3))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TNNT3 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-TNNT3 anticorps

Épitope: AA 45-251

Fonction: Anti-TNNT3 Antibody Picoband®

Réactivité croisée (Details): No cross-reactivity with other proteins.

Attributs du produit: Anti-TNNT3 Antibody Picoband® (ABIN7601762). Tested in ELISA, WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human TNNT3 recombinant protein (Position: A45-K251).

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL
ELISA, 0.1-0.5 μg/mL
1. Gurnett, C. A., Alaee, F., Desruisseau, D., Boehm, S., Dobbs, M. B. Skeletal muscle contractile gene (TNNT3, MYH3, TPM2): mutations not found in vertical talus or clubfoot. Clin. Orthop. Rel. Res. 467: 1195-1200, 2009. 2. Koch, A., Juan, T. S.-C., Jenkins, N. A., Gilbert, D. J., Copeland, N. G., McNiece, I. K., Fletcher, F. A. cDNA cloning and chromosomal mapping of mouse fast skeletal muscle troponin T. Mammalian Genome 8: 346-348, 1997.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.

Détails sur TNNT3

Antigène: TNNT3 (Fast Skeletal Troponin T (TNNT3))

Autre désignation: TNNT3

Sujet:

Synonyms: Troponin T, fast skeletal muscle, TnTf, Beta-TnTF, Fast skeletal muscle troponin T, fTnT, TNNT3

Tissue Specificity: In fetal and adult fast skeletal muscles, with a higher level expression in fetal than in adult muscle.

Background: Fast skeletal muscle troponin T (fTnT) is a protein that in humans is encoded by the TNNT3 gene. It is mapped to 11p15.5. The 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, also known as troponin T type 3. Alternative splicing results in multiple transcript variants encoding additional distinct troponin T type 3 isoforms. A developmentally regulated switch between fetal/neonatal and adult troponin T type 3 isoforms occurs. Additional splice variants have been described but their biological validity has not been established. Mutations in this gene may cause distal arthrogryposis multiplex congenita type 2B (DA2B).

Poids moléculaire: 37 kDa

ID gène: 7140

UniProt: P45378