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FACS analysis of 4% PFA-fixed U251 cells using GTX04846 SEPT9 antibody. Blue : Primary antibody Green : Isotype control Red : Unlabelled sample Permeabilized step should be included. Dilution : 1 microg/1x10? cells
FACS analysis of 4% PFA-fixed U251 cells using GTX04846 SEPT9 antibody. Blue : Primary antibody Green : Isotype control Red : Unlabelled sample Permeabilized step should be included. Dilution : 1 microg/1x10? cells
FACS analysis of 4% PFA-fixed U251 cells using GTX04846 SEPT9 antibody. Blue : Primary antibody Green : Isotype control Red : Unlabelled sample Permeabilized step should be included. Dilution : 1 microg/1x10? cells

SEPT9 antibody

GTX04846
GeneTex
ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
DownloadDatasheet
Product group Antibodies
ReactivityHuman, Mouse
TargetSEPTIN9
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Overview

  • Supplier
    GeneTex
  • Product Name
    SEPT9 antibody
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 0.25-0.5 microg/ml. ICC/IF: 5 microg/ml. IHC-P: 2-5 microg/ml. FACS: 1-3 microg/1x106 cells. ELISA: 0.1-0.5 microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Flow Cytometry, ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.5 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID10801
  • Target name
    SEPTIN9
  • Target description
    septin 9
  • Target synonyms
    AF17q25; MLL septin-like fusion protein MSF-A; MSF; MSF1; NAPB; Ov/Br septin; ovarian/breast septin; PNUTL4; SEPT9; SeptD1; septin D1; septin-9; SINT1
  • Host
    Rabbit
  • Isotype
    IgG
  • Scientific Description
    This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2009]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203