TPM3 anticorps

N° du produit ABIN5698646

L’anticorps Lapin Polyclonal anti-TPM3 a été validé pour WB, IHC, ELISA et IP. Il convient pour détecter TPM3 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour TPM3 anticorps (ABIN5698646)

Antigène: TPM3 (Tropomyosin 3 (TPM3))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TPM3 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunoprecipitation (IP)

Détail du produit anti-TPM3 anticorps

Fonction: TPM3 antibody

Immunogène: tropomyosin 3

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

mouse skeletal muscle tissue were subjected to SDS PAGE followed by western blot with FNab08890(TPM3 antibody) at dilution of 1:800

Restrictions: For Research Use only

Stockage

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

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.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur TPM3

Antigène: TPM3 (Tropomyosin 3 (TPM3))

Autre désignation: TPM3

Sujet:

Synonyms: Tropomyosin alpha-3 chain|Gamma-tropomyosin|Tropomyosin-3|Tropomyosin-5 (hTM5)|TPM3

Background: This gene encodes a member of the tropomyosin family of actin-binding proteins. Tropomyosins are dimers of coiled-coil proteins that provide stability to actin filaments and regulate access of other actin-binding proteins. Mutations in this gene result in autosomal dominant nemaline myopathy and other muscle disorders. This locus is involved in translocations with other loci, including anaplastic lymphoma receptor tyrosine kinase (ALK) and neurotrophic tyrosine kinase receptor type 1 (NTRK1), which result in the formation of fusion proteins that act as oncogenes. There are numerous pseudogenes for this gene on different chromosomes. Alternative splicing results in multiple transcript variants.

ID gène: 7169

UniProt: P06753