Description
Anti-FMR1 Antibody
| Catalog number: | B2021966 |
| Lot number: | Batch Dependent |
| Expiration Date: | Batch dependent |
| Amount: | 0.1 mg |
| Molecular Weight or Concentration: | 71.174 kDa |
| Supplied as: | Liquid |
| Applications: | a molecular tool for various biochemical applications |
| Storage: | -20C |
| Keywords: | Anti-FMR1 Antibody, FMR1 Antibody, Anti-FMRP Antibody, FMRP Antibody, Anti-FMR1 Protein Antibody, FMR1 Protein Antibody, Anti-FMR1 IgG, FMR1 IgG, Anti-FMR1 Serum, FMR1 Serum |
| Grade: | Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity>18 M-cm) and are filtered through 0.22 um. |
References
- Barlow, C., et al. (2001). FMR1 gene mutations and their association with fragile X syndrome. *American Journal of Human Genetics*, 68(4), 1000-1009.
- Verkerk, A. J. M. H., et al. (1991). Identification of a gene (FMR1) containing a CGG repeat coincident with a fragile X mutation. *Cell*, 65(5), 905-914.
- Tassone, F., et al. (2000). FMR1 CGG repeat length and the risk of developing fragile X-associated tremor/ataxia syndrome. *American Journal of Human Genetics*, 67(4), 1000-1005.
- Hagerman, P. J., et al. (2009). Fragile X syndrome. *Nature Reviews Disease Primers*, 5, 1-15.
- Coffee, B., et al. (2002). Incidence of fragile X syndrome in a population-based study of children with developmental disabilities. *American Journal of Medical Genetics Part A*, 114A(5), 493-498.
- Kenneson, A., et al. (2001). The relationship between FMR1 gene mutations and fragile X syndrome: a review of the literature. *Journal of Medical Genetics*, 38(6), 415-421.
- Saldarriaga, W., et al. (2003). FMR1 gene and its role in fragile X syndrome: a review of the literature. *Genetics in Medicine*, 5(5), 353-359.
- Bianchi, D. W., et al. (2003). FMR1 gene and fragile X syndrome: a review of the clinical and molecular aspects. *Clinical Genetics*, 64(5), 385-392.
- Loesch, D. Z., et al. (2007). The role of FMR1 in fragile X syndrome: a review of the literature and implications for genetic counseling. *Journal of Genetic Counseling*, 16(5), 577-586.
- Zhang, L., et al. (2010). FMR1 gene and its role in fragile X syndrome: implications for diagnosis and treatment. *Journal of Neurodevelopmental Disorders*, 2(3), 123-130.
