M2

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SKU: M2

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DSHB Data Sheet

Catalog Fields

Clone ID/Product Name: M2
Available to For-Profits: Yes
Alternate Antibody Name:
Gene Symbol:
Ab Isotype: RIgG2a
Gene Name:
Antibody Registry ID: AB_531785 
Uniprot ID:  
RRID:  
Entrez Gene ID:  
Clonality: Monoclonal
Immunogen: C57BL/6J mouse cerebellar homogenate
Clone:
Immunogen Sequence: Full length sequence
Myeloma Strain: P3 NSl/lAg4-1
Epitope Mapped: No
Antigen Name: M2; Astrocyte surface antigen (mouse)
Epitope Location or Sequence:
Alternate Antigen Name:
Deposit Date: 1/11/2001
Antigen Molecular Weight:
Depositor: Lagenaur, C.
Antigen Sequence:
Depositor Institution: University of Pittsburgh
Antigen Species: Mouse
Depositor Notes: The M2 antigen is detected on the cell surface of all GFA protein-positive astrocytes and immature oligodendrocytes. IHC on frozen sections post-fixed with paraformaldehyde or ethanol.
Host Species: rat
Hybridoma Cells Available (Non-Profit): Yes
Confirmed Species Reactivity: Mouse
Additional Information: RRID: AB_531785
Predicted Species Reactivity:  
Human Protein Atlas:  
Additional Characterization:  
Recommended Applications: Immunofluorescence, Immunohistochemistry
All cell products contain the antimicrobial ProClin. Click here for additional information.
These hybridomas were created by your colleagues. Please acknowledge the hybridoma contributor and the Developmental Studies Hybridoma Bank (DSHB) in the Materials and Methods of your publications. Please email the citation to us.
For your Materials & Methods section:
M2 was deposited to the DSHB by Lagenaur, C. (DSHB Hybridoma Product M2)
Storage and Handling Recommendations
Although many cell products are maintained at 4°C for years without loss of activity, shelf-life at 4°C is highly variable. For immediate use, short term storage at 4°C up to two weeks is recommended. For long term storage, divide the solution into volumes of no less than 20 ul for freezing at -20°C or -80°C. The small volume aliquot should provide sufficient reagent for short term use. Freeze-thaw cycles should be avoided. For concentrate or bioreactor products, an equal volume of glycerol, a cryoprotectant, may be added prior to freezing.
Usage Recommendations
The optimal Ig concentration for an application varies by species and antibody affinity. For each product, the antibody titer must be optimized for every application by the end user laboratory. A good starting concentration for immunohistochemistry (IHC), immunofluorescence (IF), and immunocytochemistry (ICC) when using mouse Ig is 2-5 ug/ml. For western blots, the recommended concentration range of mouse Ig 0.2-0.5 ug/ml. In general, rabbit antibodies demonstrate greater affinity and are used at a magnitude lower Ig concentration for initial testing. The recommended concentrations for rabbit Ig are 0.2-0.5 ug/ml (IF, IHC and ICC) and 20-50 ng/ml (WB).

9 References

  • Initial Publication
  • IF References
  • IHC References
  • All References
  • Initial Publication

    Monoclonal antibody (M2) to glial and neuronal cell surfaces.
    Schachner M
    Journal of supramolecular structure and cellular biochemistry 15.4 (1981): 335-46.

    IF References

    Monoclonal antibody (M2) to glial and neuronal cell surfaces.
    Schachner M
    Journal of supramolecular structure and cellular biochemistry 15.4 (1981): 335-46.

    Timing and patterns of astrocyte migration from xenogeneic transplants of the cortex and corpus callosum.
    Lund RD
    The Journal of comparative neurology 292.2 (1990 Feb 8): 320-30.

    Regulation of neural markers nestin and GFAP expression by cultivated bone marrow stromal cells.
    Rogister B
    Journal of cell science 116.Pt 16 (2003 Aug 15): 3295-302.

    Engraftment and differentiation of embryonic stem cell-derived neural progenitor cells in the cochlear nerve trunk: growth of processes into the organ of Corti.
    Edge AS
    Journal of neurobiology 66.13 (2006 Nov): 1489-500.

    miR-124 regulates adult neurogenesis in the subventricular zone stem cell niche.
    Doetsch F
    Nature neuroscience 12.4 (2009 Apr): 399-408.

    Quantitative evaluation of motor function before and after engraftment of dopaminergic neurons in a rat model of Parkinson's disease.
    Liu CS
    Journal of biomedical science 17.1 (2010 Feb 13): 9.

    Tracking differentiating neural progenitors in pluripotent cultures using microRNA-regulated lentiviral vectors.
    Jakobsson J
    Proceedings of the National Academy of Sciences of the United States of America 107.25 (2010 Jun 22): 11602-7.

    Direct conversion of fibroblasts into stably expandable neural stem cells.
    Edenhofer F
    Cell stem cell 10.4 (2012 Apr 6): 473-9.

    Humoral and contact interactions in astroglia/stem cell co-cultures in the course of glia-induced neurogenesis.
    Madarász E
    Glia 49.3 (2005 Feb): 430-44.

    IHC References
    All References

    Timing and patterns of astrocyte migration from xenogeneic transplants of the cortex and corpus callosum.
    Lund RD
    The Journal of comparative neurology 292.2 (1990 Feb 8): 320-30.

    Humoral and contact interactions in astroglia/stem cell co-cultures in the course of glia-induced neurogenesis.
    Madarász E
    Glia 49.3 (2005 Feb): 430-44.

    Monoclonal antibody (M2) to glial and neuronal cell surfaces.
    Schachner M
    Journal of supramolecular structure and cellular biochemistry 15.4 (1981): 335-46.

    Regulation of neural markers nestin and GFAP expression by cultivated bone marrow stromal cells.
    Rogister B
    Journal of cell science 116.Pt 16 (2003 Aug 15): 3295-302.

    Engraftment and differentiation of embryonic stem cell-derived neural progenitor cells in the cochlear nerve trunk: growth of processes into the organ of Corti.
    Edge AS
    Journal of neurobiology 66.13 (2006 Nov): 1489-500.

    miR-124 regulates adult neurogenesis in the subventricular zone stem cell niche.
    Doetsch F
    Nature neuroscience 12.4 (2009 Apr): 399-408.

    Quantitative evaluation of motor function before and after engraftment of dopaminergic neurons in a rat model of Parkinson's disease.
    Liu CS
    Journal of biomedical science 17.1 (2010 Feb 13): 9.

    Tracking differentiating neural progenitors in pluripotent cultures using microRNA-regulated lentiviral vectors.
    Jakobsson J
    Proceedings of the National Academy of Sciences of the United States of America 107.25 (2010 Jun 22): 11602-7.

    Direct conversion of fibroblasts into stably expandable neural stem cells.
    Edenhofer F
    Cell stem cell 10.4 (2012 Apr 6): 473-9.

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