Troponin T type 1 (slow skeletal) Antibody

Images

 
Western Blot: Troponin T type 1 (slow skeletal) Antibody [NBP1-32748] - Sample (30 ug of whole cell lysate)A: H129910% SDS PAGE, antibody diluted at 1:1000.
Immunohistochemistry-Paraffin: Troponin T type 1 (slow skeletal) Antibody [NBP1-32748] - Paraffin-embedded Porcine Skeletal muscle, using antibody at 1:500 dilution.
Immunohistochemistry-Paraffin: Troponin T type 1 (slow skeletal) Antibody [NBP1-32748] - Paraffin-embedded Colon ca, using antibody at 1:500 dilution.

Product Details

Summary
Reactivity Hu, PoSpecies Glossary
Applications WB, IHC, IHC-P
Clonality
Polyclonal
Host
Rabbit
Conjugate
Unconjugated
Concentration
0.89 mg/ml

Order Details

Troponin T type 1 (slow skeletal) Antibody Summary

Immunogen
Full length human Troponin T1 (slow skeletal) Recombinant protein.
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
TNNT1
Purity
Immunogen affinity purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Western Blot 1:500-1:3000
  • Immunohistochemistry 10 - 1:500
  • Immunohistochemistry-Paraffin 1:100-1:1000

Packaging, Storage & Formulations

Storage
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
Buffer
0.1M Tris (pH 7.0), 0.1M Glycine and 10% Glycerol
Preservative
0.01% Thimerosal
Concentration
0.89 mg/ml
Purity
Immunogen affinity purified

Alternate Names for Troponin T type 1 (slow skeletal) Antibody

  • ANMtroponin T, slow skeletal muscle
  • FLJ98147
  • MGC104241
  • Slow skeletal muscle troponin T
  • STNT
  • TnTs
  • TNTtroponin T1, skeletal, slow
  • troponin T type 1 (skeletal, slow)
  • troponin-T1, skeletal, slow

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. [provided by RefSeq]

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Bioinformatics

Gene Symbol TNNT1