TPM3 anticorps

N° du produit ABIN7257156

Détail du produit anti-TPM3 anticorps

Antigène: TPM3 (Tropomyosin 3 (TPM3))

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TPM3 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human TPM3 (NP_689476.2).

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000 IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 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.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur TPM3

Antigène: TPM3 (Tropomyosin 3 (TPM3))

Autre désignation: TPM3 (TPM3 Produits)

Synonymes: anticorps CAPM1, anticorps CFTD, anticorps NEM1, anticorps OK/SW-cl.5, anticorps TM-5, anticorps TM3, anticorps TM30, anticorps TM30nm, anticorps TM5, anticorps TPMsk3, anticorps TRK, anticorps hscp30, anticorps cb674, anticorps fa17b11, anticorps fb83b01, anticorps fk41e01, anticorps hm:zeh0298, anticorps wu:fa17b11, anticorps wu:fb83b01, anticorps wu:fk41e01, anticorps zeh0298, anticorps zgc:77592, anticorps TPM3, anticorps Tm5NM, anticorps Tpm-5, anticorps Tpm5, anticorps Trop-5, anticorps gamma-TM, anticorps hTM30nm, anticorps hTMnm, anticorps tm3, anticorps tpm3, anticorps tpm3.L, anticorps tropomyosin 3, anticorps tropomyosin 3, gamma, anticorps tropomyosin 3 S homeolog, anticorps TPM3, anticorps tpm3, anticorps Tpm3, anticorps tpm3.S

Sujet: 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.

Poids moléculaire:

Observed_MW: 37 kDa

Calculated_MW: 18 kDa/28 kDa/29 kDa/32 kDa

ID gène: 7170

UniProt: P06753