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- Antibody Data
- Antigen structure
- References [6]
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- Product number
- HPA017639 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA017639, RRID:AB_1857345
- Product name
- Anti-SNX14
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human SNX14, Gene description: sorting nexin 14, Alternative Gene Names: RGS-PX2, Validated applications: IHC, WB, Uniprot ID: Q9Y5W7, 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
- 0.1 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 Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations
Cerebellar ataxia disease–associated Snx14 promotes lipid droplet growth at ER–droplet contacts
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20
A molecular code for endosomal recycling of phosphorylated cargos by the SNX27–retromer complex
Genome sequencing reveals a splice donor site mutation in the SNX14 gene associated with a novel cerebellar cortical degeneration in the Hungarian Vizsla dog breed.
Snx14 Regulates Neuronal Excitability, Promotes Synaptic Transmission, and Is Imprinted in the Brain of Mice
Bryant D, Seda M, Peskett E, Maurer C, Pomeranz G, Ghosh M, Hawkins T, Cleak J, Datta S, Hariri H, Eckert K, Jafree D, Walsh C, Demetriou C, Ishida M, Alemán-Charlet C, Vestito L, Seselgyte R, McDonald J, Bitner-Glindzicz M, Hemberger M, Rihel J, Teboul L, Henne W, Jenkins D, Moore G, Stanier P
Scientific Reports 2020;10(1)
Scientific Reports 2020;10(1)
Cerebellar ataxia disease–associated Snx14 promotes lipid droplet growth at ER–droplet contacts
Datta S, Liu Y, Hariri H, Bowerman J, Henne W
Journal of Cell Biology 2019;218(4):1335-1351
Journal of Cell Biology 2019;218(4):1335-1351
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20
Bryant D, Liu Y, Datta S, Hariri H, Seda M, Anderson G, Peskett E, Demetriou C, Sousa S, Jenkins D, Clayton P, Bitner-Glindzicz M, Moore G, Henne W, Stanier P
Human Molecular Genetics 2018;27(11):1927-1940
Human Molecular Genetics 2018;27(11):1927-1940
A molecular code for endosomal recycling of phosphorylated cargos by the SNX27–retromer complex
Clairfeuille T, Mas C, Chan A, Yang Z, Tello-Lafoz M, Chandra M, Widagdo J, Kerr M, Paul B, Mérida I, Teasdale R, Pavlos N, Anggono V, Collins B
Nature Structural & Molecular Biology 2016;23(10):921-932
Nature Structural & Molecular Biology 2016;23(10):921-932
Genome sequencing reveals a splice donor site mutation in the SNX14 gene associated with a novel cerebellar cortical degeneration in the Hungarian Vizsla dog breed.
Fenn J, Boursnell M, Hitti RJ, Jenkins CA, Terry RL, Priestnall SL, Kenny PJ, Mellersh CS, Forman OP
BMC genetics 2016 Aug 26;17(1):123
BMC genetics 2016 Aug 26;17(1):123
Snx14 Regulates Neuronal Excitability, Promotes Synaptic Transmission, and Is Imprinted in the Brain of Mice
Adams M, Huang H, Yoon B, Brooks S, Bakal R, Berrios J, Larsen R, Wallace M, Han J, Chung E, Zylka M, Philpot B
PLoS ONE 2014;9(5):e98383
PLoS ONE 2014;9(5):e98383
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