TPM2 anticorps

N° du produit ABIN7260811

Détail du produit anti-TPM2 anticorps

Antigène: TPM2 (Tropomyosin-2 (TPM2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TPM2 est non-conjugé

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

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: A synthetic peptide of human TPM2

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:1000 IHC 1:50-1:100

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 TPM2

Antigène: TPM2 (Tropomyosin-2 (TPM2))

Autre désignation: TPM2 (TPM2 Produits)

Synonymes: anticorps CG4843, anticorps DROTROPI1, anticorps Dmel\\CG4843, anticorps Ifm(3)3, anticorps Ifm(3)5, anticorps Ifm-TmI, anticorps TM2, anticorps Tm, anticorps Tm1, anticorps Tm127, anticorps TmI, anticorps TmII, anticorps Tn-H, anticorps dro Tm, anticorps l(3)nc99Eb, anticorps mTmI, anticorps cb836, anticorps fb68h02, anticorps tpm4l, anticorps wu:fb68h02, anticorps wu:fj63f03, anticorps zgc:86810, anticorps AMCD1, anticorps DA1, anticorps DA2B, anticorps TMSB, anticorps nem4, anticorps tpm2, anticorps tpm2a, anticorps BRT-2, anticorps TPM3, anticorps NEM4, anticorps Tpm-2, anticorps Trop-2, anticorps Tropomyosin 2, anticorps Tropomyosin-2, anticorps tropomyosin, anticorps tropomyosin 2 (beta), anticorps tropomyosin 2 L homeolog, anticorps tropomyosin 2, anticorps tropomyosin 2, beta, anticorps Tm2, anticorps EDI_309330, anticorps LOC100101174, anticorps tpm2, anticorps tpm2.L, anticorps TPM2, anticorps Tpm2

Sujet: This gene encodes beta-tropomyosin, a member of the actin filament binding protein family, and mainly expressed in slow, type 1 muscle fibers. Mutations in this gene can alter the expression of other sarcomeric tropomyosin proteins, and cause cap disease, nemaline myopathy and distal arthrogryposis syndromes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Poids moléculaire:

Observed_MW: 36 kDa

Calculated_MW: 28 kDa/32 kDa

ID gène: 7169

UniProt: P07951