Titin-Cap (Telethonin) (TCAP) Peptide
TCAP
适用: 人
宿主: 合成
BP, WB
产品编号 ABIN984855
发货至:
中国
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Contact Info
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中国
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北京 101111
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Quick Overview for Titin-Cap (Telethonin) (TCAP) Peptide (ABIN984855)
抗原
TCAP
(Titin-Cap (Telethonin) (TCAP))
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-TCAP antibody (Catalog #: ARP48228_T100). 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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- TCAP (Titin-Cap (Telethonin) (TCAP))
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背景
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Sarcomere assembly is regulated by the muscle protein titin. Titin is a giant elastic protein with kinase activity that extends half the length of a sarcomere. It serves as a scaffold to which myofibrils and other muscle related proteins are attached. TCAP is a protein found in striated and cardiac muscle that binds to the titin Z1-Z2 domains and is a substrate of titin kinase, interactions thought to be critical to sarcomere assembly. Mutations in TCAP gene are associated with limb-girdle muscular dystrophy type 2G.Sarcomere assembly is regulated by the muscle protein titin. Titin is a giant elastic protein with kinase activity that extends half the length of a sarcomere. It serves as a scaffold to which myofibrils and other muscle related proteins are attached. This gene encodes a protein found in striated and cardiac muscle that binds to the titin Z1-Z2 domains and is a substrate of titin kinase, interactions thought to be critical to sarcomere assembly. Mutations in this gene are associated with limb-girdle muscular dystrophy type 2G. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: CMD1N, LGMD2G, T-cap, TELE, telethonin
Protein Interaction Partner: MYOZ1,TRIM55,TTN,ANKRD2,ATXN1,MDM2,MSTN,MYOZ1,MYOZ3,TTN,ANKRD2,MYOZ1,MYOZ2,MYOZ3,TTN
Protein Size: 167 -
分子量
- 19 kDa
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基因ID
- 8557
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NCBI登录号
- NM_003673, NP_003664
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UniProt
- O15273
抗原
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