GAD2 / GAD65 (GABAergic Neuronal Marker) Antibody, IgG1, Clone: [MSVA-602M], Mouse, Monoclonal

Artikelnummer: NBT-2572-MSM17-P1
Artikelname: GAD2 / GAD65 (GABAergic Neuronal Marker) Antibody, IgG1, Clone: [MSVA-602M], Mouse, Monoclonal
Artikelnummer: NBT-2572-MSM17-P1
Hersteller Artikelnummer: 2572-MSM17-P1
Alternativnummer: NBT-2572-MSM17-P1-100
Hersteller: NeoBiotechnologies
Wirt: Mouse
Kategorie: Antikörper
Applikation: IHC
Spezies Reaktivität: Human
Immunogen: Recombinant fragment of human GAD2 (GAD65) protein (around aa 1-200) (exact sequence is proprietary)
Alternative Synonym: DCE2, GAD2, Glutamic Acid Decarboxylase 2 (Pancreas), Glutamic Acid Decarboxylase 2 (Pancreatic Islets and Brain 65kDa), Glutamic Acid Decarboxylase 65 (GAD65)
This MAb recognizes a protein of 65kDa, which is identified as glutamic acid decarboxylase 2 (GDA2). It is responsible for catalyzing the production of gamma-aminobutyric acid from L-glutamic acid. There are two forms of glutamic acid decarboxylases (GAD s) that are found in the brain: GAD2 (also known as GAD65) and GAD1 (also known as GAD67). GAD1 and GAD2 are members of the group II decarboxylase family of proteins and are responsible for catalyzing the rate-limiting step in the production of GABA (-aminobutyric acid) from L-glutamic acid. Although both GAD s are found in the brain, GAD2 localizes to synaptic vesicle membranes in nerve terminals, while GAD1 is distributed throughout the cell. A pathogenic role for GAD2 is identified in the human pancreas since it has been identified as an autoantibody and an auto-reactive T cell target in insulin-dependent diabetes. OO
Klonalität: Monoclonal
Klon-Bezeichnung: [MSVA-602M]
Molekulargewicht: 65kDa
Isotyp: IgG1
NCBI: 2572
UniProt: Q05329
Formulierung: Ab produced in CHO cell mammalian-based expression system. Prepared in 10mM PBS with 0.05% BSA & 0.05% azide. Also available WITHOUT BSA & azide.
Glutamate decarboxylase 2 Mouse Monoclonal Antibody (MSVA-602M) tested on many normal and cancer tissues. The immunohistochemistry staining in these tissues aligns with the expression data in Human Protein Atlas.