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Mouse Anti-GAD1 Recombinant Antibody (9A6) (CBMAB-G1714-LY)


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Summary

Host Animal
Mouse
Specificity
Human
Clone
9A6
Antibody Isotype
IgG1, κ
Application
IHC, WB

Basic Information

Immunogen
Full-length recombinant human GAD65 (1-585 a.a.)
Specificity
Human
Antibody Isotype
IgG1, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Concentration
1 mg/mL
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Full Name
Glutamate Decarboxylase 1
Introduction
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. [provided by RefSeq, Jul 2008]
Entrez Gene ID
2571
UniProt ID
Q99259
Alternative Names
Glutamate Decarboxylase 1; Glutamate Decarboxylase 1 (Brain; 67kDa); Glutamate Decarboxylase 67 KDa Isoform; 7 KDa Glutamic Acid Decarboxylase; EC 4.1.1.15; GAD-67; GAD;
Function
Catalyzes the production of GABA.
Biological Process
Chemical synaptic transmission Source: ProtInc
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
Cellular Location
Plasma membrane; Axon terminus; Cell cortex; Clathrin-sculpted gamma-aminobutyric acid transport vesicle; Inhibitory synapse; Presynaptic active zone; Vesicle membrane
Involvement in disease
Cerebral palsy, spastic quadriplegic 1 (CPSQ1):
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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For research use only. Not intended for any clinical use.

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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