Antibody data
- Antibody Data
- Antigen structure
- References [3]
- Comments [0]
- Validations [0]
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Validation data
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- Product number
- HPA027051 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA027051, RRID:AB_10600915
- Product name
- Anti-TMEM199
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human TMEM199, Gene description: transmembrane protein 199, Alternative Gene Names: C17orf32, MGC45714, Validated applications: IHC, WB, Uniprot ID: Q8N511, 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
- 0.2 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 A proteome-wide map of 20(S)-hydroxycholesterol interactors in cell membranes
The vacuolar-ATPase complex and assembly factors, TMEM199 and CCDC115, control HIF1α prolyl hydroxylation by regulating cellular iron levels
TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation
Cheng Y, Zhang T, Ma X, Pratuangtham S, Zhang G, Ondrus A, Mafi A, Lomenick B, Jones J, Ondrus A
Nature Chemical Biology 2021;17(12):1271-1280
Nature Chemical Biology 2021;17(12):1271-1280
The vacuolar-ATPase complex and assembly factors, TMEM199 and CCDC115, control HIF1α prolyl hydroxylation by regulating cellular iron levels
Miles A, Burr S, Grice G, Nathan J
eLife 2017;6
eLife 2017;6
TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation
Jansen J, Timal S, van Scherpenzeel M, Michelakakis H, Vicogne D, Ashikov A, Moraitou M, Hoischen A, Huijben K, Steenbergen G, van den Boogert M, Porta F, Calvo P, Mavrikou M, Cenacchi G, van den Bogaart G, Salomon J, Holleboom A, Rodenburg R, Drenth J, Huynen M, Wevers R, Morava E, Foulquier F, Veltman J, Lefeber D
The American Journal of Human Genetics 2016;98(2):322-330
The American Journal of Human Genetics 2016;98(2):322-330
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