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Neuroscience Cell Type Marker Glia marker Oligodendrocyte marker

Anti-Olig1 antibody (ab139512)

Price and availability

284 784 ₸

Availability

Order now and get it on Wednesday March 03, 2021

Anti-Olig1 antibody (ab139512)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Rabbit polyclonal to Olig1
  • Suitable for: WB
  • Reacts with: Mouse, Rat
  • Isotype: IgG

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Overview

  • Product name

    Anti-Olig1 antibody
    See all Olig1 primary antibodies
  • Description

    Rabbit polyclonal to Olig1
  • Host species

    Rabbit
  • Tested Applications & Species

    Application Species
    WB
    Mouse
    Rat
    See all applications and species data
  • Immunogen

    Synthetic peptide within Mouse Olig1 aa 1-100 conjugated to keyhole limpet haemocyanin. The exact sequence is proprietary.
    Database link: Q9JKN5

  • Positive control

    • This antibody gave a positive signal in the following tissue lysates: Mouse Brain; Rat Brain; Mouse Cerebellum; Rat Cerebellum; Rat Oligodendrocyte Precursor Cells (OPC).

Properties

  • Form

    Liquid
  • Storage instructions

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
  • Storage buffer

    pH: 7.40
    Preservative: 0.02% Sodium azide
    Constituent: PBS

    Batches of this product that have a concentration
  • Concentration information loading...
  • Purity

    Immunogen affinity purified
  • Clonality

    Polyclonal
  • Isotype

    IgG
  • Research areas

    • Neuroscience
    • Cell Type Marker
    • Glia marker
    • Oligodendrocyte marker
    • Neuroscience
    • Neurology process
    • Neurogenesis

Associated products

  • Compatible Secondaries

    • Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077)
    • Goat Anti-Rabbit IgG H&L (HRP) (ab205718)
  • Isotype control

    • Rabbit IgG, polyclonal - Isotype Control (ChIP Grade) (ab171870)

Applications

The Abpromise guarantee

Our Abpromise guarantee covers the use of ab139512 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Guaranteed

Tested applications are guaranteed to work and covered by our Abpromise guarantee.

Predicted

Predicted to work for this combination of applications and species but not guaranteed.

Incompatible

Does not work for this combination of applications and species.

Application Species
WB
Mouse
Rat
All applications
Pig
Application Abreviews Notes
WB
Use a concentration of 1 µg/ml. Detects a band of approximately 38 kDa (predicted molecular weight: 27 kDa).
Notes
WB
Use a concentration of 1 µg/ml. Detects a band of approximately 38 kDa (predicted molecular weight: 27 kDa).

Target

  • Function

    Promotes formation and maturation of oligodendrocytes, especially within the brain. Cooperates with OLIG2 to establish the pMN domain of the embryonic neural tube.
  • Tissue specificity

    Expressed in the brain, in oligodendrocytes. Strongly expressed in oligodendrogliomas, while expression is weak to moderate in astrocytomas. Expression in glioblastomas is highly variable.
  • Sequence similarities

    Contains 1 basic helix-loop-helix (bHLH) domain.
  • Cellular localization

    Nucleus.
  • Target information above from: UniProt accession Q8TAK6 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt
  • Database links

    • Entrez Gene: 50914 Mouse
    • Entrez Gene: 60394 Rat
    • SwissProt: Q9JKN5 Mouse
    • SwissProt: Q9WUQ3 Rat
    • Unigene: 39300 Mouse
    • Unigene: 45339 Rat
    • Alternative names

      • Basic domain helix loop helix protein class B 6 antibody
      • Basic domain helix loop helix protein class B6 antibody
      • BHLH B6 antibody
      • BHLHB 6 antibody
      • bHLHb6 antibody
      • bHLHe21 antibody
      • Class B basic helix-loop-helix protein 6 antibody
      • Class E basic helix-loop-helix protein 21 antibody
      • Olig 1 antibody
      • Olig1 antibody
      • OLIG1_HUMAN antibody
      • Oligo 1 antibody
      • Oligo1 antibody
      • Oligodendrocyte lineage transcription factor 1 antibody
      • Oligodendrocyte specific bHLH transcription factor 1 antibody
      • Oligodendrocyte transcription factor 1 antibody
      see all

    Images

    • Western blot - Anti-Olig1 antibody (ab139512)
      Western blot - Anti-Olig1 antibody (ab139512)
      All lanes : Anti-Olig1 antibody (ab139512) at 1 µg/ml

      Lane 1 : Brain (Mouse) Tissue Lysate
      Lane 2 : Brain (Rat) Tissue Lysate
      Lane 3 : Rat Oligodendrocyte Precursor Cells
      Lane 4 : Cerebellum (Mouse) Tissue Lysate
      Lane 5 : Cerebellum (Rat) Tissue Lysate

      Lysates/proteins at 10 µg per lane.

      Secondary
      All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/50000 dilution

      Developed using the ECL technique.

      Performed under reducing conditions.

      Predicted band size: 27 kDa
      Observed band size: 38 kDa
      why is the actual band size different from the predicted?
      Additional bands at: 14 kDa (possible non-specific binding), 20 kDa (possible non-specific binding)


      Exposure time: 20 minutes


      This blot was produced using a 4-12% Bis-tris gel under the MES buffer system. The gel was run at 200V for 35 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 2% Bovine Serum Albumin before being incubated with ab139512 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution ab133406

    • Western blot - Anti-Olig1 antibody (ab139512)
      Western blot - Anti-Olig1 antibody (ab139512)
      All lanes : Anti-Olig1 antibody (ab139512) at 1 µg/ml (Milk blocking 3%)

      Lane 1 : Brain (Mouse) Tissue Lysate
      Lane 2 : Brain (Rat) Tissue Lysate
      Lane 3 : Cerebellum (Mouse) Tissue Lysate
      Lane 4 : Cerebellum (Rat) Tissue Lysate
      Lane 5 : Brain (Mouse) Tissue Lysate with Immunising peptide at 1 µg/ml
      Lane 6 : Brain (Rat) Tissue Lysate with Immunising peptide at 1 µg/ml
      Lane 7 : Cerebellum (Mouse) Tissue Lysate with Immunising peptide at 1 µg/ml
      Lane 8 : Cerebellum (Rat) Tissue Lysate with Immunising peptide at 1 µg/ml

      Lysates/proteins at 25 µg per lane.

      Secondary
      All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/50000 dilution

      Developed using the ECL technique.

      Performed under reducing conditions.

      Predicted band size: 27 kDa
      Observed band size: 38 kDa why is the actual band size different from the predicted?


      Exposure time: 20 minutes


      This blot was produced using a 4-12% Bis-tris gel under the MES buffer system. The gel was run at 200V for 35 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 2% Bovine Serum Albumin before being incubated with ab139512 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution ab133406

    Protocols

    • Western blot protocols

    Click here to view the general protocols

    Datasheets and documents

    • Datasheet
  • References (0)

    Publishing research using ab139512? Please let us know so that we can cite the reference in this datasheet.

    ab139512 has not yet been referenced specifically in any publications.

    Images

    • Western blot - Anti-Olig1 antibody (ab139512)
      Western blot - Anti-Olig1 antibody (ab139512)
      All lanes : Anti-Olig1 antibody (ab139512) at 1 µg/ml

      Lane 1 : Brain (Mouse) Tissue Lysate
      Lane 2 : Brain (Rat) Tissue Lysate
      Lane 3 : Rat Oligodendrocyte Precursor Cells
      Lane 4 : Cerebellum (Mouse) Tissue Lysate
      Lane 5 : Cerebellum (Rat) Tissue Lysate

      Lysates/proteins at 10 µg per lane.

      Secondary
      All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/50000 dilution

      Developed using the ECL technique.

      Performed under reducing conditions.

      Predicted band size: 27 kDa
      Observed band size: 38 kDa
      why is the actual band size different from the predicted?
      Additional bands at: 14 kDa (possible non-specific binding), 20 kDa (possible non-specific binding)


      Exposure time: 20 minutes


      This blot was produced using a 4-12% Bis-tris gel under the MES buffer system. The gel was run at 200V for 35 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 2% Bovine Serum Albumin before being incubated with ab139512 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution ab133406

    • Western blot - Anti-Olig1 antibody (ab139512)
      Western blot - Anti-Olig1 antibody (ab139512)
      All lanes : Anti-Olig1 antibody (ab139512) at 1 µg/ml (Milk blocking 3%)

      Lane 1 : Brain (Mouse) Tissue Lysate
      Lane 2 : Brain (Rat) Tissue Lysate
      Lane 3 : Cerebellum (Mouse) Tissue Lysate
      Lane 4 : Cerebellum (Rat) Tissue Lysate
      Lane 5 : Brain (Mouse) Tissue Lysate with Immunising peptide at 1 µg/ml
      Lane 6 : Brain (Rat) Tissue Lysate with Immunising peptide at 1 µg/ml
      Lane 7 : Cerebellum (Mouse) Tissue Lysate with Immunising peptide at 1 µg/ml
      Lane 8 : Cerebellum (Rat) Tissue Lysate with Immunising peptide at 1 µg/ml

      Lysates/proteins at 25 µg per lane.

      Secondary
      All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/50000 dilution

      Developed using the ECL technique.

      Performed under reducing conditions.

      Predicted band size: 27 kDa
      Observed band size: 38 kDa why is the actual band size different from the predicted?


      Exposure time: 20 minutes


      This blot was produced using a 4-12% Bis-tris gel under the MES buffer system. The gel was run at 200V for 35 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 2% Bovine Serum Albumin before being incubated with ab139512 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution ab133406

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
    For licensing inquiries, please contact partnerships@abcam.com

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