Anti-GLUD1 Antibody (CAB5176)
- SKU:
- CAB5176
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Cell Biology
Frequently bought together:
Description
抗体名: | Anti-GLUD1 Antibody |
抗体コード: | CAB5176 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB IHC IF |
反応性: | Human, Mouse, Rat |
宿主種: | Rabbit |
免疫原: | A synthesized peptide derived from human GLUD1 |
申し込み: | WB IHC IF |
推奨希釈: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200 |
反応性: | Human, Mouse, Rat |
ポジティブサンプル: | Jurkat, K-562, U-252MGMouse liver, Rat liver |
免疫原: | A synthesized peptide derived from human GLUD1 |
精製方法: | Affinity purification |
ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 0.05% BSA, 50% glycerol, pH7.3. |
アイソタイプ: | IgG |
順序: | Email for sequence |
遺伝子ID: | 2746 |
Uniprot: | P00367 |
セルラーロケーション: | |
計算された分子量: | 50kDa |
観察された分子量: | 52KDa |
同義語: | GDH, GDH1, GLUD |
バックグラウンド: | 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 |
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