Application: IHC
Clonality: Polyclonal
Host: Rabbit
Reactivity: Human
Protein Description: sperm flagellar 2
Gene Name: SPEF2
Alternative Gene Name: CT122, FLJ23577, KPL2
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000072663: 88%, ENSRNOG00000058275: 91%
Entrez Gene ID: 79925
Uniprot ID: Q9C093
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: sperm flagellar 2
Gene Name: SPEF2
Alternative Gene Name: CT122, FLJ23577, KPL2
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000072663: 88%, ENSRNOG00000058275: 91%
Entrez Gene ID: 79925
Uniprot ID: Q9C093
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 SPEF2 pAb (ATL-HPA040343 w/enhanced validation) | |
| Antigen | PrEST Antigen SPEF2 (ATL-APrEST87352) |
| Documents & Links for Anti SPEF2 pAb (ATL-HPA040343 w/enhanced validation) | |
| Datasheet | Anti SPEF2 pAb (ATL-HPA040343 w/enhanced validation) Datasheet (External Link) |
| Vendor Page | Anti SPEF2 pAb (ATL-HPA040343 w/enhanced validation) at Atlas |
| Documents & Links for Anti SPEF2 pAb (ATL-HPA040343 w/enhanced validation) | |
| Datasheet | Anti SPEF2 pAb (ATL-HPA040343 w/enhanced validation) Datasheet (External Link) |
| Vendor Page | Anti SPEF2 pAb (ATL-HPA040343 w/enhanced validation) |
| Citations for Anti SPEF2 pAb (ATL-HPA040343 w/enhanced validation) – 7 Found |
| Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice. Am J Hum Genet. 2019 Feb 7;104(2):331-340. doi: 10.1016/j.ajhg.2018.12.013. Epub 2019 Jan 24. PubMed |
| Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse. Am J Hum Genet. 2018 Apr 5;102(4):636-648. doi: 10.1016/j.ajhg.2018.03.007. PubMed |
| Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice. PLoS Genet. 2019 Aug 19;15(8):e1008315. doi: 10.1371/journal.pgen.1008315. eCollection 2019 Aug. PubMed |
| Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice. Am J Hum Genet. 2020 Sep 3;107(3):514-526. doi: 10.1016/j.ajhg.2020.07.010. Epub 2020 Aug 12. PubMed |
| Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. Am J Hum Genet. 2022 Jan 6;109(1):157-171. doi: 10.1016/j.ajhg.2021.11.022. Epub 2021 Dec 20. PubMed |
| Islet primary cilia motility controls insulin secretion. Sci Adv. 2022 Sep 23;8(38):eabq8486. doi: 10.1126/sciadv.abq8486. Epub 2022 Sep 23. PubMed |
| Novel HYDIN variants associated with male infertility in two Chinese families. Front Endocrinol (Lausanne). 2023 Jan 18;14:1118841. doi: 10.3389/fendo.2023.1118841. eCollection 2023. PubMed |