Cysteine and Glycine-Rich Protein 3 (CSRP3) Peptide
CSRP3
适用: 人
宿主: 合成
BP, WB
Quick Overview for Cysteine and Glycine-Rich Protein 3 (CSRP3) Peptide (ABIN975383)
抗原
CSRP3
(Cysteine and Glycine-Rich Protein 3 (CSRP3))
宿主
人
资源
合成
应用范围
Blocking Peptide (BP), Western Blotting (WB)
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产品特性
- 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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纯化方法
- Purified
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应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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浓度
- 1 mg/mL
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缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
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注意事项
- Avoid repeated freeze-thaw cycles.
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储存条件
- -20 °C
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储存方法
- 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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背景
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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 -
分子量
- 21 kDa
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基因ID
- 8048
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NCBI登录号
- NM_003476, NP_003467
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UniProt
- P50461
抗原
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