Cysteine and Glycine-Rich Protein 3 (CSRP3) Peptide
Aperçu rapide pour Cysteine and Glycine-Rich Protein 3 (CSRP3) Peptide (ABIN975383)
Antigène
Origine
Source
Application
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Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-CSRP3 antibody (Catalog #: ARP34181_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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Purification
- Purified
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Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Concentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- CSRP3 (Cysteine and Glycine-Rich Protein 3 (CSRP3))
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Sujet
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The 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 CSRP3 are thought to cause heritable forms of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in humans.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.
Alias Symbols: CLP, MLP, CRP3, LMO4, CMD1M, CMH12
Protein Interaction Partner: ACTN1,LDHD,MYF6,MYOD1,MYOG,NHLH1,SPTB,LDHD,MYF6,MYOD1,MYOG
Protein Size: 194 -
Poids moléculaire
- 21 kDa
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ID gène
- 8048
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NCBI Accession
- NM_003476, NP_003467
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UniProt
- P50461
Antigène
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