Mouse Anti-GAD1 Recombinant Antibody (K-87) (CBMAB-G1719-LY)

Basic Information
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Gamma-aminobutyric acid biosynthetic process Source: Ensembl
Glutamate catabolic process Source: UniProtKB
Glutamate decarboxylation to succinate Source: ProtInc
Locomotory exploration behavior Source: Ensembl
Neurotransmitter biosynthetic process Source: UniProtKB-KW
Protein-pyridoxal-5-phosphate linkage Source: UniProtKB
Response to drug Source: Ensembl
Social behavior Source: Ensembl
A non-progressive disorder of movement and/or posture resulting from defects in the developing central nervous system. Affected individuals manifest symmetrical, non-progressive spasticity and no adverse perinatal history or obvious underlying alternative diagnosis. Developmental delay, mental retardation and sometimes epilepsy can be part of the clinical picture.
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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
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Mouse Anti-GAD1 Recombinant Antibody (13k26) (CAT#: CBMAB-G1703-LY)
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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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