GeneBio Systems
Recombinant GAD-65/67 Monoclonal Antibody
Recombinant GAD-65/67 Monoclonal Antibody
SKU:AN301129L
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Size::50μL
Storage:Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping:Ice bag
Exp date:12 months
Category ID_II:Primary Antibodies
Category ID_III:Recombinant Antibodies;Monoclonal Antibodies
Abbreviation:GAD-65/67
Target Synonym:GAD;GAD2;GAD65;65 kDa glutamic acid decarboxylase;DCE 2;DCE2;GAD 2;GAD 65;GAD-2;GAD-65;Glutamate decarboxylase 2;Glutamate decarboxylase 2 (pancreas);Glutamate Decarboxylase 2 (pancreatic islets and brain 65kDa);Glutamate Decarboxylase 65;Glutamate decarboxylase 65 kDa isoform;Glutamic Acid Decarboxylase 2;Glutamic Acid Decarboxylase 65;MGC161605;MGC161607;GAD-65/67
Research Areas:Neuroscience;Metabolism
Conjugation:Unconjugated
Host:Rabbit
Species reactivity:Human;Mouse;Rat
Application:WB;IHC
Isotype:IgG,κ
Clonality:Monoclonal;Recombinant
Clone NO.:12G12
UNIProt ID:Q05329;Q99259
Accession:
Background:GAD1(glutamate decarboxylase 1) Homo sapiens This gene encodes one of several forms of glutamic acid decarboxylase, identified as a major autoantigen in insulin-dependent diabetes. The enzyme encoded is responsible for catalyzing the production of gamma-aminobutyric acid from L-glutamic acid. A pathogenic role for this enzyme has been identified in the human pancreas since it has been identified as an autoantigen and an autoreactive T cell target in insulin-dependent diabetes. This gene may also play a role in the stiff man syndrome. Deficiency in this enzyme has been shown to lead to pyridoxine dependency with seizures. Alternative splicing of this gene results in two products, the predominant 67-kD form and a less-frequent 25-kD form.
Concentration:0.2 mg/mL
Immunogen:Recombinant Human GAD-65/67 protein
Buffer:PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Purification method:Protein A
Dilution:IHC 1:200-1:1000;WB 1:10000-1:50000
Calculated MW:65 kDa,67 kDa
ObservedMW:65 kDa,67 kDa
