Rabbit anti-Human, Mouse CSRP3 Polyclonal Antibody | anti-CSRP3 antibody

CSRP3 Polyclonal Antibody

Cat. Num. AAA2537071

• Gene Names: CSRP3; CLP; MLP; CRP3; LMO4; CMD1M; CMH12
• Reactivity: Human, Mouse
• Applications: Western Blot, Immunohistochemistry
• Purity: Affinity Purification
• Synonyms: CSRP3; Polyclonal Antibody; CSRP3 Polyclonal Antibody; CLP; MLP; CRP3; LMO4; CMD1M; CMH12; anti-CSRP3 antibody

• Host: Rabbit
• Reactivity: Human, Mouse
• Clonality: Polyclonal
• Isotype: IgG
• Purity/Purification: Affinity Purification

• Applicable Applications for anti-CSRP3 antibody: Western Blot (WB), Immunohistochemistry (IHC)
• Application Notes: WB: 1:500-1:2000, IHC: 1:50-1:200
• Immunogen: Recombinant protein of human CSRP3
• Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
• Santa Cruz Alternative: Potential replacement for Santa Cruz Biotechnology antibody catalog# sc-30274 / sc-30275 / sc-98827
• Preparation and Storage: Store at -20 degree C (regular) or -80 degree C (long term). Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Western Blot (WB)

(Western blot analysis of extracts of various cell lines, using CSRP3 antibody.)

Immunohistochemistry (IHC)

(Immunohistochemistry of paraffin-embedded Mouse heart using CSRP3 antibody at dilution of1:100 (x400 lens).)

Immunofluorescence (IF3)

(Immunofluorescence analysis of HeLa cell using CSRP3 antibody. Blue: DAPI for nuclear staining.)

Related Product Information for anti-CSRP3 antibody

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.

NCBI and Uniprot Product Information

• NCBI GI #: 4502893
• NCBI GeneID: 8048
• NCBI Accession #: NP_003467.1
• NCBI GenBank Nucleotide #: NM_003476.4
• Molecular Weight: Calculated MW: 20kDa
• NCBI Official Full Name: cysteine and glycine-rich protein 3
• NCBI Official Synonym Full Names: cysteine and glycine rich protein 3
• NCBI Official Symbol: CSRP3
• NCBI Official Synonym Symbols: CLP; MLP; CRP3; LMO4; CMD1M; CMH12
• NCBI Protein Information: cysteine and glycine-rich protein 3
• UniProt Protein Name: Cysteine and glycine-rich protein 3
• Protein Family: Cysteine and glycine-rich protein
• UniProt Gene Name: CSRP3
• UniProt Synonym Gene Names: CLP; MLP; CRP3
• UniProt Entry Name: CSRP3_HUMAN

NCBI Description

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. [provided by RefSeq, Jul 2008]

Uniprot Description

CSRP3: Positive regulator of myogenesis. Plays a crucial and specific role in the organization of cytosolic structures in cardiomyocytes. Could play a role in mechanical stretch sensing. May be a scaffold protein that promotes the assembly of interacting proteins at Z-line structures. It is essential for calcineurin anchorage to the Z line. Required for stress-induced calcineurin-NFAT activation. Defects in CSRP3 are the cause of cardiomyopathy dilated type 1M (CMD1M). Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. Defects in CSRP3 are the cause of familial hypertrophic cardiomyopathy type 12 (CMH12). Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.

Protein type: Transcription regulation

Chromosomal Location of Human Ortholog: 11p15.1

Cellular Component: cytoskeleton; nucleus; Z disc

Molecular Function: actinin binding; protein binding; structural constituent of muscle; telethonin binding; zinc ion binding

Biological Process: blood vessel remodeling; cardiac muscle contraction; cardiac muscle development; cardiac myofibril assembly; cellular calcium ion homeostasis; negative regulation of myoblast differentiation; positive regulation of myoblast differentiation; positive regulation of transcription from RNA polymerase II promoter; protein localization in organelle; regulation of the force of heart contraction; skeletal muscle development

Disease: Cardiomyopathy, Dilated, 1m; Cardiomyopathy, Familial Hypertrophic, 12