Anti-GLUD1 Antibody (CAB5176)
- SKU:
- CAB5176
- Product type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Cell Biology
Frequently bought together:
Description
Antibody Name: | Anti-GLUD1 Antibody |
Antibody SKU: | CAB5176 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IHC IF |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | A synthesized peptide derived from human GLUD1 |
Application: | WB IHC IF |
Recommended Dilution: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | Jurkat, K-562, U-252MGMouse liver, Rat liver |
Immunogen: | A synthesized peptide derived from human GLUD1 |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 0.05% BSA, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | Email for sequence |
Gene ID: | 2746 |
Uniprot: | P00367 |
Cellular Location: | |
Calculated MW: | 50kDa |
Observed MW: | 52KDa |
Synonyms: | GDH, GDH1, GLUD |
Background: | This gene encodes glutamate dehydrogenase, which is a mitochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha-ketoglutarate and ammonia. This enzyme has an important role in regulating amino acid-induced insulin secretion. It is allosterically activated by ADP and inhibited by GTP and ATP. Activating mutations in this gene are a common cause of congenital hyperinsulinism. Alternative splicing of this gene results in multiple transcript variants. The related glutamate dehydrogenase 2 gene on the human X-chromosome originated from this gene via retrotransposition and encodes a soluble form of glutamate dehydrogenase. Related pseudogenes have been identified on chromosomes 10, 18 and X. [provided by RefSeq, Jan 2016] |
UniProt Protein Function: | Mitochondrial glutamate dehydrogenase that converts L-glutamate into alpha-ketoglutarate. Plays a key role in glutamine anaplerosis by producing alpha-ketoglutarate, an important intermediate in the tricarboxylic acid cycle. May be involved in learning and memory reactions by increasing the turnover of the excitatory neurotransmitter glutamate. |
NCBI Summary: | This gene encodes glutamate dehydrogenase, which is a mitochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha-ketoglutarate and ammonia. This enzyme has an important role in regulating amino acid-induced insulin secretion. It is allosterically activated by ADP and inhibited by GTP and ATP. Activating mutations in this gene are a common cause of congenital hyperinsulinism. Alternative splicing of this gene results in multiple transcript variants. The related glutamate dehydrogenase 2 gene on the human X-chromosome originated from this gene via retrotransposition and encodes a soluble form of glutamate dehydrogenase. Related pseudogenes have been identified on chromosomes 10, 18 and X. [provided by RefSeq, Jan 2016] |
UniProt Code: | P00367 |
NCBI GenInfo Identifier: | 974141156 |
NCBI Gene ID: | 2746 |
NCBI Accession: | NP_001305829.1 |
UniProt Secondary Accession: | P00367,Q5TBU3, B3KV55, B4DGN5, |
UniProt Related Accession: | P00367 |
Molecular Weight: | 46,575 Da |
NCBI Full Name: | glutamate dehydrogenase 1, mitochondrial isoform b |
NCBI Synonym Full Names: | glutamate dehydrogenase 1 |
NCBI Official Symbol: | GLUD1 |
NCBI Official Synonym Symbols: | GDH; GDH1; GLUD |
NCBI Protein Information: | glutamate dehydrogenase 1, mitochondrial |
UniProt Protein Name: | Glutamate dehydrogenase 1, mitochondrial |
UniProt Gene Name: | GLUD1 |