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antibody from antibodies-online
Targeting: ARX
CT121, EIEE1, ISSX, MRX29, MRX32, MRX33, MRX36, MRX38, MRX43, MRX54, MRX76, MRX87, MRXS1, PRTS
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- Antigen structure
- References [5]
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- Validations
- Western blot [1]
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- Product number
- ABIN950525 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-ARX (AA 39-69), (N-Term) antibody
- Antibody type
- Polyclonal
- Description
- Affinity chromatography on Protein A
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- N-Term, AA 39-69
- Vial size
- 0.4 mL
- Storage
- Store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Ohtahara syndrome in a family with an ARX protein truncation mutation (c.81C>G/p.Y27X).
ARX spectrum disorders: making inroads into the molecular pathology.
Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice.
CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy.
A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment.
Fullston T, Brueton L, Willis T, Philip S, MacPherson L, Finnis M, Gecz J, Morton J
European journal of human genetics : EJHG 2010 Feb;18(2):157-62
European journal of human genetics : EJHG 2010 Feb;18(2):157-62
ARX spectrum disorders: making inroads into the molecular pathology.
Shoubridge C, Fullston T, Gécz J
Human mutation 2010 Aug;31(8):889-900
Human mutation 2010 Aug;31(8):889-900
Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice.
Kitamura K, Itou Y, Yanazawa M, Ohsawa M, Suzuki-Migishima R, Umeki Y, Hohjoh H, Yanagawa Y, Shinba T, Itoh M, Nakamura K, Goto Y
Human molecular genetics 2009 Oct 1;18(19):3708-24
Human molecular genetics 2009 Oct 1;18(19):3708-24
CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy.
Nabbout R, Depienne C, Chipaux M, Girard B, Souville I, Trouillard O, Dulac O, Chelly J, Afenjar A, Héron D, Leguern E, Beldjord C, Bienvenu T, Bahi-Buisson N
Epilepsy research 2009 Nov;87(1):25-30
Epilepsy research 2009 Nov;87(1):25-30
A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment.
Price MG, Yoo JW, Burgess DL, Deng F, Hrachovy RA, Frost JD Jr, Noebels JL
The Journal of neuroscience : the official journal of the Society for Neuroscience 2009 Jul 8;29(27):8752-63
The Journal of neuroscience : the official journal of the Society for Neuroscience 2009 Jul 8;29(27):8752-63
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