CSRP3 anticorps

N° du produit ABIN6291316

Détail du produit anti-CSRP3 anticorps

Antigène: CSRP3 (Cysteine and Glycine-Rich Protein 3 (CSRP3))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CSRP3 est non-conjugé

Application: Immunofluorescence (IF)

Purification: Affinity purification

Immunogène: Recombinant protein of human CSRP3

Isotype: IgG

Information d'application

Indications d'application: IF 1:50 - 1:200

Commentaires:

Cardiac and slow-twitch skeletal muscles, Isoform 2 is expressed in striated muscle, Isoform 2 is specifically expressed at higher levels in patients with neuromuscular diseases, such as limb-girdle muscular dystrophy 2A (LGMD2A), Duchenne muscular dystrophy (DMD) and dermatomyositis

Restrictions: For Research Use only

Stockage

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 -20C. Avoid freeze / thaw cycles.

Détails sur CSRP3

Antigène: CSRP3 (Cysteine and Glycine-Rich Protein 3 (CSRP3))

Autre désignation: CSRP3 (CSRP3 Produits)

Synonymes: anticorps CLP, anticorps CMD1M, anticorps CMH12, anticorps CRP3, anticorps LMO4, anticorps MLP, anticorps MMLP, anticorps csrp3, anticorps zgc:103468, anticorps CSRP3, anticorps csrp3-a, anticorps cysteine and glycine rich protein 3, anticorps cysteine and glycine-rich protein 3, anticorps cysteine and glycine-rich protein 3 (cardiac LIM protein), anticorps cysteine and glycine rich protein 3 L homeolog, anticorps CSRP3, anticorps Csrp3, anticorps csrp3, anticorps csrp3.L

Sujet: This gene encodes a member of the CSRP family of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this protein is found in a group of proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Mutations in this gene are thought to cause heritable forms of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in humans. Alternatively spliced transcript variants with different 5' UTR, but encoding the same protein, have been found for this gene.

Poids moléculaire: 20.969 kDa

ID gène: 8048

UniProt: P50461