Antibody data
- Antibody Data
- Antigen structure
- References [8]
- Comments [0]
- Validations [0]
Submit
Validation data
Reference
Comment
Report error
- Product number
- 27846-1-AP - Provider product page

- Provider
- Proteintech Group
- Product name
- C22orf25 antibody
- Antibody type
- Polyclonal
- Description
- KD/KO validated C22orf25 antibody (Cat. #27846-1-AP) is a rabbit polyclonal antibody that shows reactivity with Human, Mouse and has been validated for the following applications: IHC, WB,ELISA.
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 20ul, 150ul
Submitted references TANGO2 binds crystallin alpha B and its loss causes desminopathy.
Heme allocation in eukaryotic cells relies on mitochondrial heme export through FLVCR1b to cytosolic GAPDH.
Folate as a potential treatment for lethal ventricular arrhythmias in TANGO2-deficiency disorder.
TANGO2-related rhabdomyolysis symptoms are associated with abnormal autophagy functioning.
Intrinsic and extrinsic regulation of rhabdomyolysis susceptibility by Tango2.
HRG-9 homologues regulate haem trafficking from haem-enriched compartments.
The phenotype associated with variants in TANGO2 may be explained by a dual role of the protein in ER-to-Golgi transport and at the mitochondria.
Clinical and biological characterization of 20 patients with TANGO2 deficiency indicates novel triggers of metabolic crises and no primary energetic defect.
Stentenbach M, Hughes LA, Fagan SV, Payne B, Rudler DL, Siira SJ, McCubbin T, Chopin A, Perks KL, Ermer JA, Hendry J, Er TS, Balasubramaniam S, Eliades JA, Hool LC, Packer NH, Moh ESX, Padman BS, Rackham O, Filipovska A
Nature communications 2025 Jun 6;16(1):5261
Nature communications 2025 Jun 6;16(1):5261
Heme allocation in eukaryotic cells relies on mitochondrial heme export through FLVCR1b to cytosolic GAPDH.
Jayaram DT, Sivaram P, Biswas P, Dai Y, Sweeny EA, Stuehr DJ
Nature communications 2025 Aug 26;16(1):7972
Nature communications 2025 Aug 26;16(1):7972
Folate as a potential treatment for lethal ventricular arrhythmias in TANGO2-deficiency disorder.
Xu W, Cao Y, Stephens SB, Arredondo MJ, Chen Y, Perez W, Sun L, Yu AC, Kim JJ, Lalani SR, Li N, Horrigan FT, Altamirano F, Wehrens XH, Miyake CY, Zhang L
JCI insight 2024 Jun 10;9(11)
JCI insight 2024 Jun 10;9(11)
TANGO2-related rhabdomyolysis symptoms are associated with abnormal autophagy functioning.
de Calbiac H, Montealegre S, Straube M, Renault S, Debruge H, Chentout L, Ciura S, Imbard A, Guillou EL, Marian A, Goudin N, Caccavelli L, Fabrega S, Hubas A, van Endert P, Dupont N, Diana J, Kabashi E, de Lonlay P
Autophagy reports 2024 Dec 31;3(1)
Autophagy reports 2024 Dec 31;3(1)
Intrinsic and extrinsic regulation of rhabdomyolysis susceptibility by Tango2.
Kim ES, Casey JG, Tao BS, Mansur A, Mathiyalagan N, Wallace ED, Ehrmann BM, Gupta VA
Disease models & mechanisms 2023 Sep 1;16(9)
Disease models & mechanisms 2023 Sep 1;16(9)
HRG-9 homologues regulate haem trafficking from haem-enriched compartments.
Sun F, Zhao Z, Willoughby MM, Shen S, Zhou Y, Shao Y, Kang J, Chen Y, Chen M, Yuan X, Hamza I, Reddi AR, Chen C
Nature 2022 Oct;610(7933):768-774
Nature 2022 Oct;610(7933):768-774
The phenotype associated with variants in TANGO2 may be explained by a dual role of the protein in ER-to-Golgi transport and at the mitochondria.
Milev MP, Saint-Dic D, Zardoui K, Klopstock T, Law C, Distelmaier F, Sacher M
Journal of inherited metabolic disease 2021 Mar;44(2):426-437
Journal of inherited metabolic disease 2021 Mar;44(2):426-437
Clinical and biological characterization of 20 patients with TANGO2 deficiency indicates novel triggers of metabolic crises and no primary energetic defect.
Bérat CM, Montealegre S, Wiedemann A, Nuzum MLC, Blondel A, Debruge H, Cano A, Chabrol B, Hoebeke C, Polak M, Stoupa A, Feillet F, Torre S, Boddaert N, Bruel H, Barth M, Damaj L, Abi-Wardé MT, Afenjar A, Benoist JF, Madrange M, Caccavelli L, Renard P, Hubas A, Nusbaum P, Pontoizeau C, Gobin S, van Endert P, Ottolenghi C, Maltret A, de Lonlay P
Journal of inherited metabolic disease 2021 Mar;44(2):415-425
Journal of inherited metabolic disease 2021 Mar;44(2):415-425
No comments: Submit comment
No validations: Submit validation data