Bio-Connect
ICC/IF analysis of paraformaldehyde fixed HepG2 cells using GTX24306 ALMS1 antibody. Green : Primary antibody Blue : DAPI Negative control: Unimmunized goat IgG Dilution : 10microg/ml
ICC/IF analysis of paraformaldehyde fixed HepG2 cells using GTX24306 ALMS1 antibody. Green : Primary antibody Blue : DAPI Negative control: Unimmunized goat IgG Dilution : 10microg/ml
ICC/IF analysis of paraformaldehyde fixed HepG2 cells using GTX24306 ALMS1 antibody. Green : Primary antibody Blue : DAPI Negative control: Unimmunized goat IgG Dilution : 10microg/ml

ALMS1 antibody

GTX24306
GeneTex
ApplicationsImmunoFluorescence, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetALMS1
Sign in to order and to see your custom pricing.
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    GeneTex
  • Product Name
    ALMS1 antibody
  • Delivery Days Customer
    9
  • Antibody Specificity
    The C terminus of ALMS1 shares an 8 amino acid stretch with two other human proteins: hypothetical protein (XP_169104) and ERAL1 (NP_005693). However, this stretch is located internally in these two proteins and so will most likely not cross-react with th
  • Application Supplier Note
    IHC-P: 1-3microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID7840
  • Target name
    ALMS1
  • Target description
    ALMS1 centrosome and basal body associated protein
  • Target synonyms
    ALSS; Alstrom syndrome 1; Alstrom syndrome protein 1
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ8TCU4
  • Protein Name
    Alstrom syndrome protein 1
  • Scientific Description
    This gene encodes a protein containing a large tandem-repeat domain as well as additional low complexity regions. The encoded protein functions in microtubule organization, particularly in the formation and maintanance of cilia. Mutations in this gene cause Alstrom syndrome. There is a pseudogene for this gene located adjacent in the same region of chromosome 2. Alternative splice variants have been described but their full length nature has not been determined. [provided by RefSeq, Apr 2014]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203