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Slow Skeletal Troponin T (TNNT1) (Middle Region) Peptide

TNNT1 宿主: 合成 BP, WB
产品编号 ABIN8111876
发货至: 中国
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Quick Overview for Slow Skeletal Troponin T (TNNT1) (Middle Region) Peptide (ABIN8111876)

抗原

TNNT1 (Slow Skeletal Troponin T (TNNT1))

资源

  • 4
合成

应用范围

Blocking Peptide (BP), Western Blotting (WB)
  • 蛋白结构域

    Middle Region

    原理

    TNNT1 Peptide - middle region
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    说明

    This is a synthetic peptide designed for use in combination with anti-TNNT1 antibody ( ARP42120_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. Please inquire for more details.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    缓冲液

    Lyophilized powder

    储存条件

    -20 °C

    储存方法

    For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
  • 抗原

    TNNT1 (Slow Skeletal Troponin T (TNNT1))

    背景

    Background Information: TNNT1 is a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year.This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene.

    Alternative Symbols: ANM, MGC104241, TNT, STNT, TNTS

    分子量

    33kDa

    基因ID

    7138

    NCBI登录号

    NP_003274

    UniProt

    P13805
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