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ImmunohistochemistryAntibody data
- Antibody Data
- Antigen structure
- References [3]
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- Product number
- HPA028563 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA028563, RRID:AB_10602286
- Product name
- Anti-FLAD1
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human FLAD1, Gene description: flavin adenine dinucleotide synthetase 1, Alternative Gene Names: FAD1, PP591, Validated applications: IHC, Uniprot ID: Q8NFF5, Storage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Reactivity
- Human
- 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 FLAD1‐associated multiple acyl‐CoA dehydrogenase deficiency identified by newborn screening
A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy
Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency
Muru K, Reinson K, Künnapas K, Lilleväli H, Nochi Z, Mosegaard S, Pajusalu S, Olsen R, Õunap K
Molecular Genetics & Genomic Medicine 2019;7(9)
Molecular Genetics & Genomic Medicine 2019;7(9)
A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy
Ryder B, Tolomeo M, Nochi Z, Colella M, Barile M, Olsen R, Inbar-Feigenberg M
2018;45
2018;45
Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency
Olsen R, Koňaříková E, Giancaspero T, Mosegaard S, Boczonadi V, Mataković L, Veauville-Merllié A, Terrile C, Schwarzmayr T, Haack T, Auranen M, Leone P, Galluccio M, Imbard A, Gutierrez-Rios P, Palmfeldt J, Graf E, Vianey-Saban C, Oppenheim M, Schiff M, Pichard S, Rigal O, Pyle A, Chinnery P, Konstantopoulou V, Möslinger D, Feichtinger R, Talim B, Topaloglu H, Coskun T, Gucer S, Botta A, Pegoraro E, Malena A, Vergani L, Mazzà D, Zollino M, Ghezzi D, Acquaviva C, Tyni T, Boneh A, Meitinger T, Strom T, Gregersen N, Mayr J, Horvath R, Barile M, Prokisch H
The American Journal of Human Genetics 2016;98(6):1130-1145
The American Journal of Human Genetics 2016;98(6):1130-1145
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