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IP analysis of HeLa lysates using control IgG and Dynactin 1 antibody. The precipitates were detected by the same Dynactin 1 antibody.
IP analysis of HeLa lysates using control IgG and Dynactin 1 antibody. The precipitates were detected by the same Dynactin 1 antibody.
IP analysis of HeLa lysates using control IgG and Dynactin 1 antibody. The precipitates were detected by the same Dynactin 1 antibody.

DCTN1 antibody [3D5-C6-D5]

Research Use Only
GTX49164
GeneTex
ApplicationsImmunoPrecipitation, Western Blot
Product group Antibodies
ReactivityHuman
TargetDCTN1
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Overview

  • Supplier
    GeneTex
  • Product Name
    DCTN1 antibody [3D5-C6-D5]
  • Delivery Days Customer
    9
  • Applications
    ImmunoPrecipitation, Western Blot
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    3D5-C6-D5
  • Conjugate
    Unconjugated
  • Formulation
    Liquid
  • Gene ID1639
  • Target name
    DCTN1
  • Target description
    dynactin subunit 1
  • Target synonyms
    150 kDa dynein-associated polypeptide; DAP-150; DP-150; dynactin 1 (p150, glued homolog, Drosophila); dynactin subunit 1; P135
  • Host
    Mouse
  • Isotype
    IgG2b
  • Protein IDQ14203
  • Protein Name
    Dynactin subunit 1
  • Scientific Description
    This gene encodes the largest subunit of dynactin, a macromolecular complex consisting of 10 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. Dynactin is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis. This subunit interacts with dynein intermediate chain by its domains directly binding to dynein and binds to microtubules via a highly conserved glycine-rich cytoskeleton-associated protein (CAP-Gly) domain in its N-terminus. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause distal hereditary motor neuronopathy type VIIB (HMN7B) which is also known as distal spinal and bulbar muscular atrophy (dSBMA). [provided by RefSeq, Oct 2008]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203