Application: WB, ICC, IHC
Clonality: Polyclonal
Host: Rabbit
Reactivity: Human
Protein Description: torsin A interacting protein 1
Gene Name: TOR1AIP1
Alternative Gene Name: FLJ13142, LAP1B
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000026466: 46%, ENSRNOG00000003946: 47%
Entrez Gene ID: 26092
Uniprot ID: Q5JTV8
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
Clonality: Polyclonal
Host: Rabbit
Reactivity: Human
Protein Description: torsin A interacting protein 1
Gene Name: TOR1AIP1
Alternative Gene Name: FLJ13142, LAP1B
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000026466: 46%, ENSRNOG00000003946: 47%
Entrez Gene ID: 26092
Uniprot ID: Q5JTV8
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
| Cognate Antibody/Antigen for Anti TOR1AIP1 pAb (ATL-HPA050546 w/enhanced validation) | |
| Antigen | PrEST Antigen TOR1AIP1 (ATL-APrEST83561) |
| Documents & Links for Anti TOR1AIP1 pAb (ATL-HPA050546 w/enhanced validation) | |
| Datasheet | Anti TOR1AIP1 pAb (ATL-HPA050546 w/enhanced validation) Datasheet (External Link) |
| Vendor Page | Anti TOR1AIP1 pAb (ATL-HPA050546 w/enhanced validation) at Atlas |
| Documents & Links for Anti TOR1AIP1 pAb (ATL-HPA050546 w/enhanced validation) | |
| Datasheet | Anti TOR1AIP1 pAb (ATL-HPA050546 w/enhanced validation) Datasheet (External Link) |
| Vendor Page | Anti TOR1AIP1 pAb (ATL-HPA050546 w/enhanced validation) |
| Citations for Anti TOR1AIP1 pAb (ATL-HPA050546 w/enhanced validation) – 3 Found |
| Two novel cases further expand the phenotype of TOR1AIP1-associated nuclear envelopathies. Hum Genet. 2020 Apr;139(4):483-498. doi: 10.1007/s00439-019-02105-6. Epub 2020 Feb 13. PubMed |
| Nuclear Accumulation of LAP1:TRF2 Complex during DNA Damage Response Uncovers a Novel Role for LAP1. Cells. 2020 Jul 29;9(8):1804. doi: 10.3390/cells9081804. PubMed |
| Congenital myasthenic syndrome due to a TOR1AIP1 mutation: a new disease pathway for impaired synaptic transmission. Brain Commun. 2020 Oct 18;2(2):fcaa174. doi: 10.1093/braincomms/fcaa174. eCollection 2020. PubMed |