Antibody data
- Antibody Data
- Antigen structure
- References [4]
- Comments [0]
- Validations [0]
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Validation data
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- Product number
- HPA029926 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA029926, RRID:AB_10602173
- Product name
- Anti-COA7
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human COA7, Gene description: cytochrome c oxidase assembly factor 7 (putative), Alternative Gene Names: C1orf163, FLJ12439, RESA1, SELRC1, Validated applications: ICC, IHC, WB, Uniprot ID: Q96BR5, Storage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 100 µl
- Concentration
- 0.3 mg/ml
- Storage
- Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Handling
- The antibody solution should be gently mixed before use.
Submitted references OCIAD1 and prohibitins regulate the stability of the TIM23 protein translocase
Ovarian carcinoma immunoreactive antigen–like protein 2 (OCIAD2) is a novel complex III–specific assembly factor in mitochondria
Inhibition of proteasome rescues a pathogenic variant of respiratory chain assembly factor COA7
Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy
Elancheliyan P, Maruszczak K, Serwa R, Stephan T, Gulgec A, Borrero-Landazabal M, Ngati S, Gosk A, Jakobs S, Wasilewski M, Chacinska A
Cell Reports 2024;43(12):115038
Cell Reports 2024;43(12):115038
Ovarian carcinoma immunoreactive antigen–like protein 2 (OCIAD2) is a novel complex III–specific assembly factor in mitochondria
Chojnacka K, Elancheliyan P, Mussulini B, Mohanraj K, Callegari S, Gosk A, Banach T, Góral T, Szczepanowska K, Rehling P, Serwa R, Chacinska A, Ott M
Molecular Biology of the Cell 2022;33(4)
Molecular Biology of the Cell 2022;33(4)
Inhibition of proteasome rescues a pathogenic variant of respiratory chain assembly factor COA7
Mohanraj K, Wasilewski M, Benincá C, Cysewski D, Poznanski J, Sakowska P, Bugajska Z, Deckers M, Dennerlein S, Fernandez‐Vizarra E, Rehling P, Dadlez M, Zeviani M, Chacinska A
EMBO Molecular Medicine 2019;11(5)
EMBO Molecular Medicine 2019;11(5)
Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy
Higuchi Y, Okunushi R, Hara T, Hashiguchi A, Yuan J, Yoshimura A, Murayama K, Ohtake A, Ando M, Hiramatsu Y, Ishihara S, Tanabe H, Okamoto Y, Matsuura E, Ueda T, Toda T, Yamashita S, Yamada K, Koide T, Yaguchi H, Mitsui J, Ishiura H, Yoshimura J, Doi K, Morishita S, Sato K, Nakagawa M, Yamaguchi M, Tsuji S, Takashima H
Brain 2018;141(6):1622-1636
Brain 2018;141(6):1622-1636
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