Anti-MT-ATP6 Antibody (CAB18315)
- SKU:
- CAB18315
- Product type:
- Antibody
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
Frequently bought together:
Description
| 抗体名: | Anti-MT-ATP6 Antibody |
| 抗体コード: | CAB18315 |
| 抗体サイズ: | 20uL, 50uL, 100uL |
| 申し込み: | WB IF |
| 反応性: | Mouse, Rat |
| 宿主種: | Rabbit |
| 免疫原: | Recombinant protein of human MT-ATP6. |
| 申し込み: | WB IF |
| 推奨希釈: | WB 1:500 - 1:2000 IF 1:50 - 1:200 |
| 反応性: | Mouse, Rat |
| ポジティブサンプル: |
| 免疫原: | Recombinant protein of human MT-ATP6. |
| 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, 50% glycerol, pH7.3. |
| アイソタイプ: | IgG |
| 順序: | Email for sequence |
| 遺伝子ID: | 4508 |
| Uniprot: | P00846 |
| セルラーロケーション: | |
| 計算された分子量: | 25kDa |
| 観察された分子量: |
 | Immunofluorescence - MT-ATP6 Rabbit pAb (CAB18315) |
| 同義語: | ATPase6, MTATP6, MT-ATP6 |
| バックグラウンド: |
| UniProt Protein Function: | ATP6: Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Key component of the proton channel; it may play a direct role in the translocation of protons across the membrane. Defects in MT-ATP6 are the cause of neurogenic muscle weakness, ataxia, and retinitis pigmentosa (NARP). Defects in MT-ATP6 are a cause of Leber hereditary optic neuropathy (LHON). LHON is a maternally inherited disease resulting in acute or subacute loss of central vision, due to optic nerve dysfunction. Cardiac conduction defects and neurological defects have also been described in some patients. LHON results from primary mitochondrial DNA mutations affecting the respiratory chain complexes. Defects in MT-ATP6 are a cause of Leigh syndrome (LS). LS is a severe neurological disorder characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions. Defects in MT-ATP6 are a cause of mitochondrial infantile bilateral striatal necrosis (MIBSN). Bilateral striatal necrosis is a neurological disorder resembling Leigh syndrome. Belongs to the ATPase A chain family. |
| UniProt Protein Details: | Protein type:Transporter, ion channel; Membrane protein, integral; Mitochondrial; Membrane protein, multi-pass; Transporter Chromosomal Location of Human Ortholog: - Disease: Neuropathy, Ataxia, And Retinitis Pigmentosa; Leber Optic Atrophy |
| UniProt Code: | P00846 |
| NCBI GenInfo Identifier: | 251831112 |
| NCBI Gene ID: | 4508 |
| NCBI Accession: | YP_003024031.1 |
| UniProt Secondary Accession: | P00846,Q34772, Q5S8W5, Q5S9E7, Q5S9I6, Q5SA31, Q6RPB7 Q6VHC0, Q6VHE0, Q6WQF4, Q7YCC1, Q7YCF8, |
| Molecular Weight: | 25kDa |
| NCBI Full Name: | ATP synthase F0 subunit 6 (mitochondrion) |
| NCBI Synonym Full Names: | mitochondrially encoded ATP synthase 6 |
| NCBI Official Symbol: | MT-ATP6 |
| NCBI Official Synonym Symbols: | ATPase6; MTATP6; ATP6 |
| NCBI Protein Information: | ATP synthase F0 subunit 6 |
| UniProt Protein Name: | ATP synthase subunit a |
| UniProt Synonym Protein Names: | F-ATPase protein 6 |
| UniProt Gene Name: | MT-ATP6 |
| UniProt Entry Name: | ATP6_HUMAN |
Related Products
Anti-MT-ND1 Antibody (CAB9743)
€0.00
概要抗体名:MT-ND1 Rabbit mAb抗体コード:CAB9743サイズ:20uL, 50uL, 100uL同義語:MTND1申し込み:WB反応性:Mouse
