Mouse Anti-EMX2 Recombinant Antibody (CBFYE-0839) (V2LY-0825-LY187)
Basic Information
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Brain development Source: GO_Central
Cell proliferation in forebrain Source: Ensembl
Central nervous system development Source: GO_Central
Cerebral cortex regionalization Source: Ensembl
Dentate gyrus development Source: Ensembl
Forebrain cell migration Source: Ensembl
Neuron differentiation Source: GO_Central
Regulation of transcription by RNA polymerase II Source: GO_Central
Response to drug Source: Ensembl
Ureter morphogenesis Source: Ensembl
Extremely rare human congenital disorder characterized by a full-thickness cleft within the cerebral hemispheres. These clefts are lined with gray matter and most commonly involve the parasylvian regions. Large portions of the cerebral hemispheres may be absent and replaced by cerebro-spinal fluid.
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme Linked Immunospot (ELISpot)
Proteogenomic
Other Protocols
Related Products
Mouse Anti-EMX2 Recombinant Antibody (CBFYE-0838) (CAT#: V2LY-0825-LY186)
Mouse Anti-EMX2 Recombinant Antibody (4D8) (CAT#: V2LY-0825-LY190)
Mouse Anti-EMX2 Recombinant Antibody (3C11) (CAT#: V2LY-0825-LY189)
Mouse Anti-EMX2 Recombinant Antibody (CBFYE-0837) (CAT#: CBMAB-E1292-FY)
Custom Antibody Labeling
We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).
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