Antibody data
- Antibody Data
- Antigen structure
- References [3]
- Comments [0]
- Validations [0]
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Validation data
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- Product number
- HPA039951 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA039951, RRID:AB_10795300
- Product name
- Anti-TBCK
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human TBCK, Gene description: TBC1 domain containing kinase, Alternative Gene Names: HSPC302, MGC16169, Validated applications: WB, IHC, Uniprot ID: Q8TEA7, Storage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Reactivity
- Human
- 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 Heterozygous variants in TBCK cause a mild neurologic syndrome in humans and mice
In vivo identification of GTPase interactors by mitochondrial relocalization and proximity biotinylation
Recessive Inactivating Mutations in TBCK, Encoding a Rab GTPase-Activating Protein, Cause Severe Infantile Syndromic Encephalopathy
Nair D, Diaz‐Rosado A, Varella‐Branco E, Ramos I, Black A, Angireddy R, Park J, Murali S, Yoon A, Ciesielski B, O'Brien W, Passos‐Bueno M, Bhoj E
American Journal of Medical Genetics Part A 2023;191(10):2508-2517
American Journal of Medical Genetics Part A 2023;191(10):2508-2517
In vivo identification of GTPase interactors by mitochondrial relocalization and proximity biotinylation
Gillingham A, Bertram J, Begum F, Munro S
eLife 2019;8
eLife 2019;8
Recessive Inactivating Mutations in TBCK, Encoding a Rab GTPase-Activating Protein, Cause Severe Infantile Syndromic Encephalopathy
Chong J, Caputo V, Phelps I, Stella L, Worgan L, Dempsey J, Nguyen A, Leuzzi V, Webster R, Pizzuti A, Marvin C, Ishak G, Ardern-Holmes S, Richmond Z, Bamshad M, Ortiz-Gonzalez X, Tartaglia M, Chopra M, Doherty D
The American Journal of Human Genetics 2016;98(4):772-781
The American Journal of Human Genetics 2016;98(4):772-781
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