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Key Documents

F6304

Sigma-Aldrich

Anti-FOXP2 antibody produced in rabbit

IgG fraction of antiserum, buffered aqueous solution

Synonyme(s) :

Anti-CAGH44, Anti-Forkhead Box P2, Anti-SPCH1, Anti-Speech and Language Disorder 1, Anti-TNRC10, Anti-Trinucleotide Repeat Containing 10

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About This Item

Numéro MDL:
Code UNSPSC :
12352203
Nomenclature NACRES :
NA.41

Source biologique

rabbit

Conjugué

unconjugated

Forme d'anticorps

IgG fraction of antiserum

Type de produit anticorps

primary antibodies

Clone

polyclonal

Forme

buffered aqueous solution

Poids mol.

antigen ~80 kDa

Espèces réactives

human, mouse, rat

Technique(s)

microarray: suitable
western blot: 1:500-1:1,000 using extracts of Jurkat cells
western blot: 1:500-1:1,000 using mouse heart tissue extract

Numéro d'accès UniProt

Conditions d'expédition

dry ice

Température de stockage

−20°C

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... FOXP2(93986)
mouse ... Foxp2(114142)

Description générale

The superfamily of Forkhead transcription factors (FOX) consists of more than 100 members, with orthologues expressed in a variety of species ranging from yeast to man. They are characterized by a common Forkhead (or winged helix) domain, a variant of the helix-turnhelix motif. Forkhead box P2 (FOXP2) transcripts encode for three different isoforms, I, II and III encoding for proteins of 715, 740, and 623 amino acids respectively. FOXP2 has a polyglutamine tract. FOXP1, FOXP2 and FOXP4 contain a complex N-terminal region responsible for transcriptional repression. This region contains various protein-protein interaction motifs conserved in all three proteins, including a zinc finger and a putative leucine zipper.

Immunogène

synthetic peptide corresponding to amino acids 36-53 of human FOXP2, conjugated to KLH via a C-terminal lysine residue. The immunizing sequence is conserved in mouse and rat.

Application

Anti-FOXP2 antibody is suitable for:
  • western blot analysis as primary antibody of the embryonic cortex to study the expression of FoxP2 in neural precursors of the embryonic cortex.
  • immunohistochemistry of prostate gland cells to determine the expression level of FOXP2 in prostate cancer.
  • microarray
  • western blot at a dilution of 1:500-1:1,000 using extracts of Jurkat cells and mouse heart tissue extract.

Actions biochimiques/physiologiques

Forkhead box P2 (FOXP2) is the first gene relevant to the human ability to develop language, offering an opportunity to study neural mechanisms from a molecular perspective. Missense and nonsense mutations have been identifying in families with language impairment. Thus, a point mutation led to the isolation to FOXP2, whereas more recently a truncation was discovered in a family with speech and language difficulties as well.
Forkhead transcription factors (FOX) family consists of more than 100 members. It is widely expressed in a variety of species ranging from yeast to man. It has a common Forkhead (or Winged Helix) domain, a variant of the helix-turnhelix motif. It plays a key regulatory role in embryonic development, differentiation, apoptosis and tumorigenesis. Its subfamily P (FOXP1, FOXP2, FOXP3 and FOXP4) has well defined clinical implications in tumor suppression as well as autoimmunity and development. FOXP2 is composed of a polyglutamine tract and a complex N-terminal region responsible for transcriptional repression. The N-terminal region contains various protein-protein interaction motifs including a zinc finger and a putative leucine zipper. It has been reported that FOXP2 acts as a major part of a multiprotein complex that regulates diverse aspects of tissue restricted gene expression during development.

Forme physique

Solution in 0.01 M phosphate buffered saline, pH 7.4, and 15 mM sodium azide.

Clause de non-responsabilité

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits
MacDermot KD, et al.
American Journal of Human Genetics, 76(6), 1074-1074 (2005)
Ogyi Park et al.
Annals of the New York Academy of Sciences, 1051, 218-228 (2005-08-30)
Crohn's disease (CD) is a chronic inflammatory bowel disease typified by transmural inflammation affecting any part of the gastrointestinal tract. CD4(+)CD25(+) regulatory T cells (T(reg) cells) play important roles in intestinal homeostasis. Adoptive transfer of regulatory T cells into mice
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder
Lai CSL, et al.
Brain, 126(Pt), 11-11 (2003)
David Tsui et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 33(1), 244-258 (2013-01-04)
The transcription factor FoxP2 has been associated with the development of human speech but the underlying cellular function of FoxP2 is still unclear. Here we provide evidence that FoxP2 regulates genesis of some intermediate progenitors and neurons in the mammalian
A forkhead-domain gene is mutated in a severe speech and language disorder.
Lai CS
Nature, 413(6855), 519-523 (2001)

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