Product Name
Forkhead Box Protein P2 (FOXP2), ELISA Kit
Full Product Name
Donkey Forkhead Box Protein P2 (FOXP2) ELISA Kit
Product Gene Name
FOXP2 elisa kit
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
Request Current Manual
Species Reactivity
Donkey
Preparation and Storage
Store all reagents at 2-8 degree C
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of FOXP2 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Searchable Terms for FOXP2 purchase
MBS9347481 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Forkhead Box Protein P2 (FOXP2) ELISA Kit target analytes in
biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing FOXP2. The ELISA analytical biochemical technique of the MBS9347481 kit is based on FOXP2 antibody-FOXP2 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect FOXP2 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, FOXP2. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
NCBI/Uniprot data below describe general gene information for FOXP2. It may not necessarily be applicable to this product.
NCBI Accession #
NP_683698.2
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NCBI GenBank Nucleotide #
NM_148900.3
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UniProt Secondary Accession #
Q6ZND1; Q75MJ3; Q8IZE0; Q8N0W2; Q8N6B7; Q8N6B8; Q8NFQ1; A0AUV6; A4D0U8; A6NNW4; B4DLD9[Other Products]
UniProt Related Accession #
O15409[Other Products]
Molecular Weight
81,840 Da
NCBI Official Full Name
forkhead box protein P2 isoform IV
NCBI Official Synonym Full Names
forkhead box P2
NCBI Official Symbol
FOXP2 [Similar Products]
NCBI Official Synonym Symbols
SPCH1; CAGH44; TNRC10
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NCBI Protein Information
forkhead box protein P2
UniProt Protein Name
Forkhead box protein P2
UniProt Synonym Protein Names
CAG repeat protein 44; Trinucleotide repeat-containing gene 10 protein
Protein Family
Forkhead box protein
UniProt Gene Name
FOXP2 [Similar Products]
UniProt Synonym Gene Names
CAGH44; TNRC10 [Similar Products]
UniProt Entry Name
FOXP2_HUMAN
NCBI Summary for FOXP2
This gene encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and ***** 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.[provided by RefSeq, Feb 2010]
UniProt Comments for FOXP2
FOXP2: Transcriptional repressor that may play a role in the specification and differentiation of lung epithelium. May also play a role in developing neural, gastrointestinal and cardiovascular tissues. Can act with CTBP1 to synergistically repress transcription but CTPBP1 is not essential. Involved in neural mechanisms mediating the development of speech and language. Forms homodimers and heterodimers with FOXP1 and FOXP4. Dimerization is required for DNA-binding. Interacts with CTBP1. Isoform 1 and isoform 6 are expressed in ***** and fetal brain, caudate nucleus and lung. 9 isoforms of the human protein are produced by alternative splicing.
Protein type: DNA-binding; C2H2-type zinc finger protein
Chromosomal Location of Human Ortholog: 7q31
Cellular Component: nucleus
Molecular Function: DNA binding; metal ion binding; protein binding; protein heterodimerization activity; protein homodimerization activity; sequence-specific DNA binding; transcription factor activity
Biological Process: alveolus development; anatomical structure morphogenesis; camera-type eye development; caudate nucleus development; cell differentiation; cerebellum development; cerebral cortex development; growth; negative regulation of transcription from RNA polymerase II promoter; negative regulation of transcription, DNA-dependent; positive regulation of mesenchymal cell proliferation; post-embryonic development; putamen development; righting reflex; skeletal muscle development; smooth muscle development; transcription, DNA-dependent; vocal learning
Disease: Speech-language Disorder 1
Research Articles on FOXP2
1. TBR1 homodimerizes; it interacts with FOXP2, a transcription factor implicated in speech/language disorders, and this interaction is disrupted by pathogenic mutations affecting either protein
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