Application: ICC, IHC
Clonality: Polyclonal
Host: Rabbit
Reactivity: Human
Protein Description: distal-less homeobox 5
Gene Name: DLX5
Alternative Gene Name:
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000029755: 93%, ENSRNOG00000010905: 92%
Entrez Gene ID: 1749
Uniprot ID: P56178
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: distal-less homeobox 5
Gene Name: DLX5
Alternative Gene Name:
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000029755: 93%, ENSRNOG00000010905: 92%
Entrez Gene ID: 1749
Uniprot ID: P56178
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 DLX5 pAb (ATL-HPA005670) | |
| Antigen | PrEST Antigen DLX5 (ATL-APrEST86924) |
| Documents & Links for Anti DLX5 pAb (ATL-HPA005670) | |
| Datasheet | Anti DLX5 pAb (ATL-HPA005670) Datasheet (External Link) |
| Vendor Page | Anti DLX5 pAb (ATL-HPA005670) at Atlas |
| Documents & Links for Anti DLX5 pAb (ATL-HPA005670) | |
| Datasheet | Anti DLX5 pAb (ATL-HPA005670) Datasheet (External Link) |
| Vendor Page | Anti DLX5 pAb (ATL-HPA005670) |
| Citations for Anti DLX5 pAb (ATL-HPA005670) – 4 Found |
| Human intermediate progenitor diversity during cortical development. Proc Natl Acad Sci U S A. 2021 Jun 29;118(26):e2019415118. doi: 10.1073/pnas.2019415118. PubMed |
| Distal-less homeobox genes Dlx5/6 regulate Müllerian duct regression. Front Endocrinol (Lausanne). 2022 Jul 15;13:916173. doi: 10.3389/fendo.2022.916173. eCollection 2022. PubMed |
| Immunofluorescence and fluorescent-protein tagging show high correlation for protein localization in mammalian cells. Nat Methods. 2013 Apr;10(4):315-23. doi: 10.1038/nmeth.2377. Epub 2013 Feb 24. PubMed |
| Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis. PLoS Genet. 2016 Sep 13;12(9):e1006307. doi: 10.1371/journal.pgen.1006307. eCollection 2016 Sep. PubMed |