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- Product number
- ABIN952403 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Fukutin (FKTN) (AA 184-214), (Middle Region) antibody
- Antibody type
- Polyclonal
- Description
- Protein A column, followed by peptide affinity purification
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Epitope
- AA 184-214, Middle Region
- Vial size
- 0.4 mL
- Storage
- Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Fukutin mutations in congenital muscular dystrophies with defective glycosylation of dystroglycan in Korea.
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study.
Fukutin gene mutations in an Italian patient with early onset muscular dystrophy but no central nervous system involvement.
Founder Fukutin mutation causes Walker-Warburg syndrome in four Ashkenazi Jewish families.
Lim BC, Ki CS, Kim JW, Cho A, Kim MJ, Hwang H, Kim KJ, Hwang YS, Park WY, Lim YJ, Kim IO, Lee JS, Chae JH
Neuromuscular disorders : NMD 2010 Aug;20(8):524-30
Neuromuscular disorders : NMD 2010 Aug;20(8):524-30
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study.
Mercuri E, Messina S, Bruno C, Mora M, Pegoraro E, Comi GP, D'Amico A, Aiello C, Biancheri R, Berardinelli A, Boffi P, Cassandrini D, Laverda A, Moggio M, Morandi L, Moroni I, Pane M, Pezzani R, Pichiecchio A, Pini A, Minetti C, Mongini T, Mottarelli E, Ricci E, Ruggieri A, Saredi S, Scuderi C, Tessa A, Toscano A, Tortorella G, Trevisan CP, Uggetti C, Vasco G, Santorelli FM, Bertini E
Neurology 2009 May 26;72(21):1802-9
Neurology 2009 May 26;72(21):1802-9
Fukutin gene mutations in an Italian patient with early onset muscular dystrophy but no central nervous system involvement.
Saredi S, Ruggieri A, Mottarelli E, Ardissone A, Zanotti S, Farina L, Morandi L, Mora M, Moroni I
Muscle & nerve 2009 Jun;39(6):845-8
Muscle & nerve 2009 Jun;39(6):845-8
Founder Fukutin mutation causes Walker-Warburg syndrome in four Ashkenazi Jewish families.
Chang W, Winder TL, LeDuc CA, Simpson LL, Millar WS, Dungan J, Ginsberg N, Plaga S, Moore SA, Chung WK
Prenatal diagnosis 2009 Jun;29(6):560-9
Prenatal diagnosis 2009 Jun;29(6):560-9
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Supportive validation
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- antibodies-online (provider)
- Main image
- Experimental details
- WB
Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- IHC
