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- References [4]
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- Product number
- ABIN357797 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Methyl CpG Binding Protein 2 (MECP2) antibody
- Antibody type
- Polyclonal
- Description
- Protein A Chromatography followed by peptide affinity purification.
- Reactivity
- Human, Mouse
- Host
- Rabbit
- 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 The A140V mutation in the MECP2 gene is not a common etiological factor among Brazilian mentally retarded males.
MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism.
Expression of Dnmt1, demethylase, MeCP2 and methylation of tumor-related genes in human gastric cancer.
Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome.
dos Santos JM, Abdalla CB, Campos M Jr, Santos-Rebouças CB, Pimentel MM
Neuroscience letters 2005 Apr 29;379(1):13-6
Neuroscience letters 2005 Apr 29;379(1):13-6
MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism.
Shibayama A, Cook EH Jr, Feng J, Glanzmann C, Yan J, Craddock N, Jones IR, Goldman D, Heston LL, Sommer SS
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004 Jul 1;128B(1):50-3
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004 Jul 1;128B(1):50-3
Expression of Dnmt1, demethylase, MeCP2 and methylation of tumor-related genes in human gastric cancer.
Fang JY, Cheng ZH, Chen YX, Lu R, Yang L, Zhu HY, Lu LG
World journal of gastroenterology 2004 Dec 1;10(23):3394-8
World journal of gastroenterology 2004 Dec 1;10(23):3394-8
Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome.
Schanen C, Houwink EJ, Dorrani N, Lane J, Everett R, Feng A, Cantor RM, Percy A
American journal of medical genetics. Part A 2004 Apr 15;126A(2):129-40
American journal of medical genetics. Part A 2004 Apr 15;126A(2):129-40
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