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TNNT1 antibody

The Rabbit Polyclonal anti-TNNT1 antibody has been validated for WB, IHC and ELISA. It is suitable to detect TNNT1 in samples from Human and Mouse.
Catalog No. ABIN7254007

Quick Overview for TNNT1 antibody (ABIN7254007)

Target

See all TNNT1 Antibodies
TNNT1 (Slow Skeletal Troponin T (TNNT1))

Reactivity

  • 22
  • 9
  • 8
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 24
  • 6
  • 1
Rabbit

Clonality

  • 27
  • 4
Polyclonal

Conjugate

  • 24
  • 4
  • 3
This TNNT1 antibody is un-conjugated

Application

  • 31
  • 19
  • 15
  • 12
  • 4
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human TNNT1

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, IHC 1:25-1:50, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.66 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    TNNT1 (Slow Skeletal Troponin T (TNNT1))

    Alternative Name

    TNNT1

    Background

    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.

    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 33 kDa

    UniProt

    P13805
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