Anti FLAD1 pAb (ATL-HPA028563)
Atlas Antibodies
- Catalog No.:
- ATL-HPA028563-25
- Shipping:
- Calculated at Checkout
$303.00
Gene Name: FLAD1
Alternative Gene Name: FAD1, PP591
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000042642: 90%, ENSRNOG00000020642: 90%
Entrez Gene ID: 80308
Uniprot ID: Q8NFF5
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.
Product Specifications | |
Application | IHC |
Reactivity | Human |
Clonality | Polyclonal |
Host | Rabbit |
Immunogen | RTDPYSCSLCPFSPTDPGWPAFMRINPLLDWTYRDIWDFLRQLFVPYCILYDRGYTSLGSRENTVRNPALKCLSPGGHPTYRPAYLLENEE |
Gene Sequence | RTDPYSCSLCPFSPTDPGWPAFMRINPLLDWTYRDIWDFLRQLFVPYCILYDRGYTSLGSRENTVRNPALKCLSPGGHPTYRPAYLLENEE |
Gene ID - Mouse | ENSMUSG00000042642 |
Gene ID - Rat | ENSRNOG00000020642 |
Buffer | 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative. |
Documents & Links for Anti FLAD1 pAb (ATL-HPA028563) | |
Datasheet | Anti FLAD1 pAb (ATL-HPA028563) Datasheet (External Link) |
Vendor Page | Anti FLAD1 pAb (ATL-HPA028563) at Atlas Antibodies |
Documents & Links for Anti FLAD1 pAb (ATL-HPA028563) | |
Datasheet | Anti FLAD1 pAb (ATL-HPA028563) Datasheet (External Link) |
Vendor Page | Anti FLAD1 pAb (ATL-HPA028563) |
Citations for Anti FLAD1 pAb (ATL-HPA028563) – 3 Found |
Ryder, B; Tolomeo, M; Nochi, Z; Colella, M; Barile, M; Olsen, R K; Inbar-Feigenberg, M. A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy. Jimd Reports. 45( 30311138):37-44. PubMed |
Olsen, Rikke K J; Koňaříková, Eliška; Giancaspero, Teresa A; Mosegaard, Signe; Boczonadi, Veronika; Mataković, Lavinija; Veauville-Merllié, Alice; Terrile, Caterina; Schwarzmayr, Thomas; Haack, Tobias B; Auranen, Mari; Leone, Piero; Galluccio, Michele; Imbard, Apolline; Gutierrez-Rios, Purificacion; Palmfeldt, Johan; Graf, Elisabeth; Vianey-Saban, Christine; Oppenheim, Marcus; Schiff, Manuel; Pichard, Samia; Rigal, Odile; Pyle, Angela; Chinnery, Patrick F; Konstantopoulou, Vassiliki; Möslinger, Dorothea; Feichtinger, René G; Talim, Beril; Topaloglu, Haluk; Coskun, Turgay; Gucer, Safak; Botta, Annalisa; Pegoraro, Elena; Malena, Adriana; Vergani, Lodovica; Mazzà, Daniela; Zollino, Marcella; Ghezzi, Daniele; Acquaviva, Cecile; Tyni, Tiina; Boneh, Avihu; Meitinger, Thomas; Strom, Tim M; Gregersen, Niels; Mayr, Johannes A; Horvath, Rita; Barile, Maria; Prokisch, Holger. Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency. American Journal Of Human Genetics. 2016;98(6):1130-1145. PubMed |
Muru, Kai; Reinson, Karit; Künnapas, Kadi; Lilleväli, Hardo; Nochi, Zahra; Mosegaard, Signe; Pajusalu, Sander; Olsen, Rikke K J; Õunap, Katrin. FLAD1-associated multiple acyl-CoA dehydrogenase deficiency identified by newborn screening. Molecular Genetics & Genomic Medicine. 2019;7(9):e915. PubMed |