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IP analysis of MCF-7 cell lysate using GTX54021 DCTN1 antibody. Antibody amount : 3microg / 200microg lysate Dilution : 1:1000
IP analysis of MCF-7 cell lysate using GTX54021 DCTN1 antibody. Antibody amount : 3microg / 200microg lysate Dilution : 1:1000
IP analysis of MCF-7 cell lysate using GTX54021 DCTN1 antibody. Antibody amount : 3microg / 200microg lysate Dilution : 1:1000

DCTN1 antibody

GTX54021
GeneTex
ApplicationsImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetDCTN1
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Overview

  • Supplier
    GeneTex
  • Product Name
    DCTN1 antibody
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 1:500 - 1:2000. ICC/IF: 1:20 - 1:100. IP: 1:50 - 1:100. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • 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
    Rabbit
  • Isotype
    IgG
  • 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, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203