Forkhead Box P2 (FOXP2) ELISA Kits

FOXP2 encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. Zusätzlich bieten wir Ihnen FOXP2 Antikörper (131) und FOXP2 Proteine (6) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
Anti-Human FOXP2 FOXP2 93986 O15409
Anti-Maus FOXP2 FOXP2 114142 P58463
Anti-Ratte FOXP2 FOXP2 500037 P0CF24
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Weitere ELISA Kits für FOXP2 Interaktionspartner

Human Forkhead Box P2 (FOXP2) Interaktionspartner

  1. Increased frequency of FOXP2 expression significantly correlated with FOXP1 (zeige FOXP1 ELISA Kits)-positivity, and FOXP1 (zeige FOXP1 ELISA Kits) co-immunoprecipitated FOXP2 from activated B-cell-diffuse large B-cell lymphoma (ABC (zeige ABCB6 ELISA Kits)-DLBCL) cells.

  2. These findings suggest that miR (zeige MLXIP ELISA Kits)-139 plays a suppressive role in the regulation of osteosarcoma cell proliferation and migration via directly targeting FOXP2.

  3. results provide evidence that FOXP2 SNPs influence aspects of human inner speech and fluency that are related to lateralized phenotypes, and suggest that the evolution of human language, as mediated by the adaptive evolution of FOXP2, involved features of inner speech

  4. An intragenic deletion in FOXP2.

  5. The proposes a binding model for the FOXP2 FHD that involves three types of binding sequence: low affinity sites which allow for rapid scanning of the genome by the protein in a partially unstructured state; moderate affinity sites which serve to locate the protein near target sites and high-affinity sites which secure the protein to the DNA .

  6. FOXP2 can be modified with all three human SUMO proteins and that PIAS1 (zeige PIAS1 ELISA Kits) promotes this process.

  7. FOXP2 is a substrate for SUMOylation and SUMOylation of FOXP2 plays a functional role in regulating its transcriptional activity.

  8. CNTNAP2 (zeige CNTNAP2 ELISA Kits) is transcriptionally regulated by FOXP2.

  9. Data suggest FOXP2 binds DNA as monomer; FOXP2 hinge loop domain mutants exhibit either decreased formation of homodimer (A539P) or decreased dissociation of homodimer (F541C); naturally occurring reverse mutation (P539A) increases DNA binding affinity.

  10. Genetic variants in FOXP2 may be significant for rare forms of language impairment, they do not contribute appreciably to individual variation in the normal range as found in the general population.

Mouse (Murine) Forkhead Box P2 (FOXP2) Interaktionspartner

  1. Eesults indicate a role of FoxP2 differential expression in cell morphology control of the vertebrate telencephalon.

  2. that Foxp2-Mef2C (zeige MEF2C ELISA Kits) signaling is critical to corticostriatal circuit formation

  3. Sumoylation of forkhead box P2 in neonatal mouse cerebellum regulates Purkinje cell development and motor functions and vocal communication, demonstrating evidence for sumoylation in regulating mammalian behaviors.

  4. we demonstrated for the first time that Foxp1 (zeige FOXP1 ELISA Kits) and Foxp2 are expressed during craniofacial development. Our data suggest that the Foxp genes may regulate development of the aboral and posterior regions of the jaw.

  5. Combined loss of all three Foxp1 (zeige FOXP1 ELISA Kits)/2/4 family members in the developing anterior foregut endoderm leads to a loss of lung endoderm lineage commitment and subsequent development. Foxp1 (zeige FOXP1 ELISA Kits)/2/4 deficient lungs express high levels of transcriptional regulators not normally expressed in developing lung. Ectopic expression of these transcriptional regulators is accompanied by decreased expression of lung restricted transcription.

  6. We show that Foxp1 (zeige FOXP1 ELISA Kits) and the androgen receptor (zeige AR ELISA Kits) are co-expressed in striatal medium spiny neurons and that brain-specific (zeige CALY ELISA Kits) androgen receptor (zeige AR ELISA Kits) KO (ArNesCre) mice exhibit reduced Foxp1 (zeige FOXP1 ELISA Kits) expression in the striatum at E17.5 and P7.5 and an increased Foxp2 level in the cortex at P7.5. Thus, androgens may contribute to sex-specific differences in Foxp1 (zeige FOXP1 ELISA Kits) and Foxp2 expression and ultrasonic vocalizations

  7. The Foxp2 gene is critical for normal vocal behavior in juvenile and adult mice.

  8. This study demonstrated that after middle cerebral artery occlusion mice demonstrate profoundly impaired socially evoked USVs and suppression of the language-associated transcription factor, Forkhead box protein 2 (Foxp2).

  9. mice with Foxp2 mutations displayed quantitative differences in ultrasonic vocalizations as compared to wild-types

  10. Collectively, these findings reveal an important role for the FOXP1 (zeige FOXP1 ELISA Kits), 2, and 4 proteins in governing postnatal alpha cell expansion and function.

Zebrafish Forkhead Box P2 (FOXP2) Interaktionspartner

  1. Our findings suggest that foxP2 is not necessary for axon pathfinding during development.

  2. foxP2 likely has a more general conserved role in nervous system development; molecular cloning

  3. The developing optic tectum becomes the major area of FoxP2 expression. In the adult brain, the highest concentrations of the FoxP2 transcript can be observed in the optic tectum.

  4. Domain-specific regulation of foxP2 CNS expression by lef1 (zeige LEF1 ELISA Kits).

FOXP2 Antigen-Profil

Beschreibung des Gens

This gene encodes 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.

Genbezeichner und Symbole assoziert mit Forkhead Box P2 (FOXP2) ELISA Kits

  • forkhead box P2 (FOXP2) Antikörper
  • forkhead box P2 (Foxp2) Antikörper
  • forkhead box P2 (foxp2) Antikörper
  • forkhead box P2 (foxP2) Antikörper
  • lmw-gs (Foxp2) Antikörper
  • forkhead box transcription factor (foxp1c) Antikörper
  • forkhead box P2 L homeolog (foxp2.L) Antikörper
  • 2810043D05Rik Antikörper
  • AI449000 Antikörper
  • CAG-16 Antikörper
  • cagh44 Antikörper
  • D0Kist7 Antikörper
  • foxP Antikörper
  • Foxp2 Antikörper
  • foxp2a Antikörper
  • foxP2b Antikörper
  • RGD1559697 Antikörper
  • spch1 Antikörper
  • tnrc10 Antikörper
  • xlFoxP2 Antikörper

Bezeichner auf Proteinebene für Forkhead Box P2 (FOXP2) ELISA Kits

CAG repeat protein 44 , forkhead box protein P2 , forkhead/winged-helix transcription factor , trinucleotide repeat containing 10 , trinucleotide repeat-containing gene 10 protein , forkhead box P2 , transcription factor FoxP2 , forkhead box P protein , lmw-gs , forkhead box transcription factor , xlFoxP2

93986 Homo sapiens
114142 Mus musculus
449627 Pan troglodytes
482413 Canis lupus familiaris
500037 Rattus norvegicus
505502 Bos taurus
555242 Danio rerio
613237 Macaca mulatta
751769 Taeniopygia guttata
769935 Gallus gallus
100101742 Xenopus (Silurana) tropicalis
100127352 Sus scrofa
100134847 Felis catus
100137387 Papio anubis
100144325 Oryctolagus cuniculus
100169841 Oryzias latipes
100303474 Saccoglossus kowalevskii
542882 Triticum aestivum
779033 Xenopus laevis
100439724 Pongo abelii
734154 Xenopus laevis
100990292 Pan paniscus
100717297 Cavia porcellus
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