FOXP2 Antibody

ProSci
Product Code: PSI-62-036
Product Group: Primary Antibodies
Supplier: ProSci
CodeSizePrice
PSI-62-036-400ul400ul£626.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Host Type: Rabbit
Antibody Isotype: Rabbit Ig
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species:
  • Human
  • Mouse
Applications:
  • Immunofluorescence (IF)
  • Western Blot (WB)
Storage:
Store at 4˚C for three months and -20˚C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Images

1 / 2
Western blot analysis in mouse heart tissue lysates (15ug/lane).This demonstrates the detected FOXP2 protein (arrow).
2 / 2
Confocal immunofluorescent analysis of FOXP2 Antibody with HepG2 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).

Western blot analysis in mouse heart tissue lysates (15ug/lane).This demonstrates the detected FOXP2 protein (arrow).
Confocal immunofluorescent analysis of FOXP2 Antibody with HepG2 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).

Further Information

Additional Names:
Forkhead box protein P2, CAG repeat protein 44, Trinucleotide repeat-containing gene 10 protein, FOXP2, CAGH44, TNRC10
Application Note:
For WB starting dilution is: 1:1000

For IF starting dilution is: 1:10~50
Background:
FOXP2 is a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Multiple alternative transcripts encoding different isoforms have been identified in this gene.
Background References:
  • Lai, C.S., et al. Nature 413(6855):519-523(2001) Lai, C.S., et al. Am. J. Hum. Genet. 67(2):357-368(2000) Margolis, R.L., et al. Hum. Genet. 100(1):114-122(1997) Hurst, J.A., et al. Dev Med Child Neurol 32(4):352-355(1990)
Buffer:
Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration:
batch dependent
Conjugate:
Unconjugated
DISCLAIMER:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.
Homology:
Predicted species reactivity based on immunogen sequence: Rat
Immunogen:
This FOXP2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 657-684 amino acids from the C-terminal region of human FOXP2.
NCBI Gene ID #:
93986
NCBI Official Name:
Forkhead box protein P2
NCBI Official Symbol:
FOXP2
NCBI Organism:
Homo sapiens
Physical State:
Liquid
PREDICTED MOLECULAR WEIGHT:
80 kDa
Protein Accession #:
O15409
Purification:
This antibody is purified through a protein A column, followed by peptide affinity purification.
Swissprot #:
O15409
User NOte:
Optimal dilutions for each application to be determined by the researcher.