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- References [10]
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- Product number
- 11973-1-AP - Provider product page
- Provider
- Proteintech Group
- Proper citation
- Proteintech Cat#11973-1-AP, RRID:AB_2287228
- Product name
- TIMM13 antibody
- Antibody type
- Polyclonal
- Description
- TIMM13 antibody (Cat. #11973-1-AP) is a rabbit polyclonal antibody that shows reactivity with human and has been validated for the following applications: IF, IHC, WB,ELISA.
- Reactivity
- Human
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 20ul, 150ul
Submitted references Targeting prohibitins activates the ISR through DELE1-HRI by impairing protein import into the mitochondrial matrix.
TIMM8A-TIMM13 Complex Exerts Oncogenic Functions in Lung Cancer.
DDX49 as a novel prognostic biomarker regulates colorectal cancer cell proliferation through the TIMM44-PI3K-AKT pathway.
In depth profiling of dihydrolipoamide dehydrogenase deficiency in primary patients fibroblasts reveals metabolic reprogramming secondary to mitochondrial dysfunction.
Human Tim8a, Tim8b and Tim13 are auxiliary assembly factors of mature Complex IV.
Functional analysis of a novel mutation in the TIMM8A gene that causes deafness-dystonia-optic neuronopathy syndrome.
Disrupting Mitochondrial Copper Distribution Inhibits Leukemic Stem Cell Self-Renewal.
Function of hTim8a in complex IV assembly in neuronal cells provides insight into pathomechanism underlying Mohr-Tranebjærg syndrome.
TIM29 is a subunit of the human carrier translocase required for protein transport.
The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency.
Sánchez-Vera I, Cosialls AM, Maritorena-Hualde N, Schuler MH, Lavilla R, Pons G, Jae LT, Iglesias-Serret D, Gil J
Cell death and differentiation 2026 May;33(5):1081-1095
Cell death and differentiation 2026 May;33(5):1081-1095
TIMM8A-TIMM13 Complex Exerts Oncogenic Functions in Lung Cancer.
Li S, Shi K, Wang Y, Zhang Y
Oncology research 2025;33(9):2435-2449
Oncology research 2025;33(9):2435-2449
DDX49 as a novel prognostic biomarker regulates colorectal cancer cell proliferation through the TIMM44-PI3K-AKT pathway.
Huang B, Yin Z, Gao G, Li L, Yang M
Frontiers in oncology 2025;15:1707092
Frontiers in oncology 2025;15:1707092
In depth profiling of dihydrolipoamide dehydrogenase deficiency in primary patients fibroblasts reveals metabolic reprogramming secondary to mitochondrial dysfunction.
Sprecher U, Dsouza J, Marisat M, Barasch D, Mishra K, Kakhlon O, Manor J, Anikster Y, Weil M
Molecular genetics and metabolism reports 2025 Mar;42:101172
Molecular genetics and metabolism reports 2025 Mar;42:101172
Human Tim8a, Tim8b and Tim13 are auxiliary assembly factors of mature Complex IV.
Anderson AJ, Crameri JJ, Ang CS, Malcolm TR, Kang Y, Baker MJ, Palmer CS, Sharpe AJ, Formosa LE, Ganio K, Baker MJ, McDevitt CA, Ryan MT, Maher MJ, Stojanovski D
EMBO reports 2023 Aug 3;24(8):e56430
EMBO reports 2023 Aug 3;24(8):e56430
Functional analysis of a novel mutation in the TIMM8A gene that causes deafness-dystonia-optic neuronopathy syndrome.
Neighbors A, Moss T, Holloway L, Yu SH, Annese F, Skinner S, Saneto R, Steet R
Molecular genetics & genomic medicine 2020 Mar;8(3):e1121
Molecular genetics & genomic medicine 2020 Mar;8(3):e1121
Disrupting Mitochondrial Copper Distribution Inhibits Leukemic Stem Cell Self-Renewal.
Singh RP, Jeyaraju DV, Voisin V, Hurren R, Xu C, Hawley JR, Barghout SH, Khan DH, Gronda M, Wang X, Jitkova Y, Sharon D, Liyanagae S, MacLean N, Seneviratene AK, Mirali S, Borenstein A, Thomas GE, Soriano J, Orouji E, Minden MD, Arruda A, Chan SM, Bader GD, Lupien M, Schimmer AD
Cell stem cell 2020 Jun 4;26(6):926-937.e10
Cell stem cell 2020 Jun 4;26(6):926-937.e10
Function of hTim8a in complex IV assembly in neuronal cells provides insight into pathomechanism underlying Mohr-Tranebjærg syndrome.
Kang Y, Anderson AJ, Jackson TD, Palmer CS, De Souza DP, Fujihara KM, Stait T, Frazier AE, Clemons NJ, Tull D, Thorburn DR, McConville MJ, Ryan MT, Stroud DA, Stojanovski D
eLife 2019 Nov 4;8
eLife 2019 Nov 4;8
TIM29 is a subunit of the human carrier translocase required for protein transport.
Callegari S, Richter F, Chojnacka K, Jans DC, Lorenzi I, Pacheu-Grau D, Jakobs S, Lenz C, Urlaub H, Dudek J, Chacinska A, Rehling P
FEBS letters 2016 Dec;590(23):4147-4158
FEBS letters 2016 Dec;590(23):4147-4158
The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency.
Di Fonzo A, Ronchi D, Lodi T, Fassone E, Tigano M, Lamperti C, Corti S, Bordoni A, Fortunato F, Nizzardo M, Napoli L, Donadoni C, Salani S, Saladino F, Moggio M, Bresolin N, Ferrero I, Comi GP
American journal of human genetics 2009 May;84(5):594-604
American journal of human genetics 2009 May;84(5):594-604
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Supportive validation
- Submitted by
- Proteintech Group (provider)
- Main image
- Experimental details
- The TIMM13 antibody from Proteintech is a rabbit polyclonal antibody to a recombinant protein of human TIMM13. This antibody recognizes human, mouse, rat antigen. The TIMM13 antibody has been validated for the following applications: ELISA, WB analysis.
