GRID2 antibody (AA 800-880)
Quick Overview for GRID2 antibody (AA 800-880) (ABIN7221306)
Target
See all GRID2 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 800-880
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Purpose
- Rabbit Anti-GluR-δ2 Polyclonal Antibody
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Specificity
- GluR-δ2 Polyclonal Antibody detects endogenous levels of GluR-δ2 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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Immunogen
- Synthesized peptide derived from the C-terminal region of human GluR-delta2 at AA range: 800-880
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,IF 1:200-1:1000,ELISA 1:20000,Not yet tested in other applications.
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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Expiry Date
- 12 months
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- GRID2 (Glutamate Receptor, Ionotropic, delta 2 (GRID2))
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Alternative Name
- GluR-delta2
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Background
- GRID2, GLURD2, Glutamate receptor delta-2 subunit, GluR delta-2 subunitThe glutamate ionotropic receptor delta type subunit 2 encoded by GRID2 is a member of the family of ionotropic glutamate receptors which are the predominant excitatory neurotransmitter receptors in the mammalian brain. The encoded protein is a multi-pass membrane protein that is expressed selectively in cerebellar Purkinje cells. A point mutation in the mouse ortholog, associated with the phenotype named 'lurcher', in the heterozygous state leads to ataxia resulting from selective, cell-autonomous apoptosis of cerebellar Purkinje cells during postnatal development. Mice homozygous for this mutation die shortly after birth from massive loss of mid- and hindbrain neurons during late embryogenesis. This protein also plays a role in synapse organization between parallel fibers and Purkinje cells. Alternate splicing results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause cerebellar ataxia in humans.
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Molecular Weight
- 113kD
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Gene ID
- 2895
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UniProt
- O43424
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Pathways
- Synaptic Membrane
Target
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