Antibody data
- Antibody Data
- Antigen structure
- References [3]
- Comments [0]
- Validations [0]
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Validation data
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- Product number
- HPA046816 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA046816, RRID:AB_2679822
- Product name
- Anti-ATAT1
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human ATAT1, Gene description: alpha tubulin acetyltransferase 1, Alternative Gene Names: C6orf134, Em:AB023049.7, FLJ13158, MEC17, Validated applications: IHC, Uniprot ID: Q5SQI0, 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
- 0.6 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 Membrane-Associated α-Tubulin Is Less Acetylated in Postmortem Prefrontal Cortex from Depressed Subjects Relative to Controls: Cytoskeletal Dynamics, HDAC6, and Depression
Glucocorticoids rapidly inhibit cell migration through a novel, non-transcriptional HDAC6 pathway.
ATAT1-enriched vesicles promote microtubule acetylation via axonal transport
Singh H, Chmura J, Bhaumik R, Pandey G, Rasenick M
The Journal of Neuroscience 2020;40(20):4033-4041
The Journal of Neuroscience 2020;40(20):4033-4041
Glucocorticoids rapidly inhibit cell migration through a novel, non-transcriptional HDAC6 pathway.
Kershaw S, Morgan DJ, Boyd J, Spiller DG, Kitchen G, Zindy E, Iqbal M, Rattray M, Sanderson CM, Brass A, Jorgensen C, Hussell T, Matthews LC, Ray DW
Journal of cell science 2020 Jun 11;133(11)
Journal of cell science 2020 Jun 11;133(11)
ATAT1-enriched vesicles promote microtubule acetylation via axonal transport
Even A, Morelli G, Broix L, Scaramuzzino C, Turchetto S, Gladwyn-Ng I, Le Bail R, Shilian M, Freeman S, Magiera M, Jijumon A, Krusy N, Malgrange B, Brone B, Dietrich P, Dragatsis I, Janke C, Saudou F, Weil M, Nguyen L
Science Advances 2019;5(12)
Science Advances 2019;5(12)
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