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Mouse Anti-GAD1 Recombinant Antibody (5D8) (CBMAB-1552-CN)

This product is a mouse antibody that recognizes GAD1 of human. The antibody 5D8 can be used for immunoassay techniques such as: WB, IHC.
See all GAD1 antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
5D8
Antibody Isotype
IgG1
Application
WB, IHC

Basic Information

Immunogen
A protein expressed in 293T cell transfected with human GAD1 expression vector
Specificity
Human
Antibody Isotype
IgG1
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
Buffer
PBS, pH 7.3, 1% BSA, 50% Glycerol
Preservative
0.02% Sodium azide
Concentration
1 mg/mL
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
Glutamate Decarboxylase 1
Introduction
GAD1 is identified as a major autoantigen in insulin-dependent diabetes, which 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. GAD1 may also play a role in the stiff man syndrome and deficiency in GAD1 has been shown to lead to pyridoxine dependency with seizures.
Entrez Gene ID
2571
UniProt ID
Q99259
Alternative Names
GAD; SCP; CPSQ1
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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