Goat Anti-FOXG1 / BF2 Antibody

P55316

WB, IF, ICC, E

Epilepsy in Rett syndrome: Clinical and genetic features. Pintaudi M, et al. Epilepsy Behav, 2010 Aug 20. PMID 20728410.
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant. Bahi-Buisson N, et al. Neurogenetics, 2010 May. PMID 19806373.
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome. Mencarelli MA, et al. J Med Genet, 2010 Jan. PMID 19578037.
Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females. Philippe C, et al. J Med Genet, 2010 Jan. PMID 19564653.
FOXG1 is responsible for the congenital variant of Rett syndrome. Ariani F, et al. Am J Hum Genet, 2008 Jul. PMID 18571142.

2290

Peptide-affinity purified goat antibody

AF1430a (0.3 µg/ml) staining of Human Brain lysate (35 µg protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.

NP_005240; 2290; 15228 (mouse); 24370 (rat);

100ug/200ul