TNNT1 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00007138-T01

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Size:100 uL
Price: USD $ 247.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot
QC Test

Western Blot

Lane 1: TNNT1 transfected lysate ( 27.61 KDa)
Lane 2: Non-transfected lysate.

SDS-PAGE Gel
QC Test

SDS-PAGE Gel

TNNT1 transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-TNNT1 full-length

    Host

    Human

    Theoretical MW (kDa)

    9.13

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-TNNT1 antibody (H00007138-B01) by Western Blots.

    Western Blot

    Lane 1: TNNT1 transfected lysate ( 27.61 KDa)
    Lane 2: Non-transfected lysate.

    SDS-PAGE Gel

    TNNT1 transfected lysate.

    Storage Buffer

    1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot

  • Gene Info — TNNT1

    Entrez GeneID

    7138

    GeneBank Accession#

    NM_003283

    Protein Accession#

    NP_003274

    Gene Name

    TNNT1

    Gene Alias

    ANM, FLJ98147, MGC104241, STNT, TNT, TNTS

    Gene Description

    troponin T type 1 (skeletal, slow)

    Omim ID

    191041 605355

    Gene Ontology

    Hyperlink

    Gene Summary

    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

    Other Designations

    slow skeletal muscle troponin T|troponin T1, skeletal, slow|troponin-T1, skeletal, slow

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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