AffiAB® Anti-FOXG1 Antibody
FoxG1 Syndrome is characterized by microcephaly and brain malformations. It affects most aspects of development and can cause seizures. FOXG1 syndrome is classified as an autism spectrum disorder and was previously considered a variant of Rett syndrome.
Antibody type
Rabbit polyclonal Antibody
Uniprot ID
SwissProt: P55316 Human; SwissProt: Q60987 Mouse
Recombinant
NO
Conjugation
Non-conjugated
Host
Rabbit
Isotype
IgG
Clone
N/A
KO/KD
N/A
Species reactivity
Human, Mouse
Tested applications
WB, IHC-P
Predicted species reactivity
N/A
Immunogen
Synthetic peptide within human FOXG1 aa 430-485.
Storage
Store at +4°C after thawing. Aliquot store at -20°C. Avoid repeated freeze / thaw cycles.
Form
Liquid
Storage buffer
1*TBS (pH7.4) , 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration
1 mg/mL.
Purity
Immunogen affinity purified.
Signal pathway
N/A
Recommended dilutions
WB: 1:500-1:2, 000; IHC-P: 1:50-1:200
Molecular Weight
Predicted band size:52 kDa.
Subcellular location
Nucleus.
Positive control
Mouse brain tissue lysate, SHSY5Y cell lysate, SHG-44 cell lysate, human skin tissue.