CSRP3 anticorps (C-Term)

N° du produit ABIN2778312

Détail du produit anti-CSRP3 anticorps

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

Épitope: C-Term

Reactivité: Humain, Souris, Rat, Chien, Boeuf (Vache), Lapin, Cheval, Cobaye

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CSRP3 est non-conjugé

Application: Western Blotting (WB)

Séquence: FRCAICGKSL ESTNVTDKDG ELYCKVCYAK NFGPTGIGFG GLTQQVEKKE

Homologie: Cow: 93%, Dog: 100%, Guinea Pig: 93%, Horse: 93%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 93%

Attributs du produit: This is a rabbit polyclonal antibody against CSRP3. It was validated on Western Blot using a cell lysate as a positive control.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the C terminal region of human CSRP3

Information d'application

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

Commentaires:

Antigen size: 194 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur CSRP3

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

Autre désignation: CSRP3 (CSRP3 Produits)

Sujet: This CSRP3 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.
Alias Symbols: CLP, MLP, CRP3, LMO4, CMD1M, CMH12
Protein Interaction Partner: UBC, HDAC4, LDHD, SPTB, NHLH1, MYF6, MYOG, MYOD1, ACTN1,
Protein Size: 194

Poids moléculaire: 21 kDa

ID gène: 8048

NCBI Accession: NM_003476, NP_003467

UniProt: P50461