NNT Antibody (PACO10882)
- SKU:
- PACO10882
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- WB
- Application:
- IHC
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
抗体名: | NNT Antibody (PACO10882) |
抗体コード: | PACO10882 |
サイズ: | 50ul |
宿主種: | Rabbit |
申し込み: | ELISA, WB, IHC |
推奨される希釈: | |
反応性: | Human, Mouse, Rat |
免疫原: | Human NNT |
憲法: | Liquid |
ストレージバッファ: | PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles. |
精製方法: | Antigen Affinity Purified |
抗体のクローン性: | Polyclonal |
アイソタイプ: | IgG |
Conjugate: | Non-conjugated |
シノニム: | nicotinamide nucleotide transhydrogenase;NNT;MGC126502;MGC126503 ; |
UniProt Protein Function: | NNT: The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane. May play a role in reactive oxygen species (ROS) detoxification in the adrenal gland. Defects in NNT are the cause of glucocorticoid deficiency type 4 (GCCD4). A rare, potentially lethal, autosomal recessive disorder characterized by resistance to ACTH action on the adrenal cortex, adrenal insufficiency and an inability of the adrenal cortex to produce cortisol. It usually presents in the neonatal period or in early childhood with episodes of hypoglycemia and other symptoms related to cortisol deficiency, including failure to thrive, recurrent illnesses or infections, convulsions, and shock. In a small number of patients hypoglycemia can be sufficiently severe and persistent that it leads to serious long-term neurological damage or death. The diagnosis is readily confirmed with a low plasma cortisol measurement in the presence of an elevated ACTH level, and normal aldosterone and plasma renin measurements. |
UniProt Protein Details: | Protein type:Cofactor and Vitamin Metabolism - nicotinate and nicotinamide; Mitochondrial; EC 1.6.1.2; Membrane protein, integral; Oxidoreductase; Membrane protein, multi-pass Chromosomal Location of Human Ortholog: 5p12 Cellular Component: mitochondrion; membrane; mitochondrial inner membrane; integral to membrane; mitochondrial respiratory chain Molecular Function:NAD(P) transhydrogenase activity; NAD(P)+ transhydrogenase (AB-specific) activity; NADP binding; NAD binding; NAD(P)+ transhydrogenase (B-specific) activity Biological Process: cellular metabolic process; proton transport; cell redox homeostasis; tricarboxylic acid cycle Disease: Glucocorticoid Deficiency 4 |
NCBI Summary: | This gene encodes an integral protein of the inner mitochondrial membrane. The enzyme couples hydride transfer between NAD(H) and NADP(+) to proton translocation across the inner mitochondrial membrane. Under most physiological conditions, the enzyme uses energy from the mitochondrial proton gradient to produce high concentrations of NADPH. The resulting NADPH is used for biosynthesis and in free radical detoxification. Two alternatively spliced variants, encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008] |
UniProt Code: | Q13423 |
NCBI GenInfo Identifier: | 51338801 |
NCBI Gene ID: | 23530 |
NCBI Accession: | Q13423.3 |
UniProt Secondary Accession: | Q13423,Q16796, Q2TB60, Q8N3V4, |
UniProt Related Accession: | Q13423 |
Molecular Weight: | 1086 |
NCBI Full Name: | NAD(P) transhydrogenase, mitochondrial |
NCBI Synonym Full Names: | nicotinamide nucleotide transhydrogenase |
NCBI Official Symbol: | NNT |
NCBI Official Synonym Symbols: | GCCD4 |
NCBI Protein Information: | NAD(P) transhydrogenase, mitochondrial; NAD(P) transhydrogenase, mitochondrial; pyridine nucleotide transhydrogenase |
UniProt Protein Name: | NAD(P) transhydrogenase, mitochondrial |
UniProt Synonym Protein Names: | Nicotinamide nucleotide transhydrogenase; Pyridine nucleotide transhydrogenase |
Protein Family: | NAD(P) transhydrogenase |
UniProt Gene Name: | NNT |
UniProt Entry Name: | NNTM_HUMAN |