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Recombinant Rabbit Anti-FOXP2 Monoclonal Antibody
Recombinant Rabbit Anti-FOXP2 Monoclonal Antibody
CAGH44; SPCH1; TNRC10; 2810043D05Rik; CAG-16; D0Kist7; RGD1559697; FOXP2_HUMAN; FOXP2; CAG repeat protein 44; Trinucleotide repeat-containing gene 10 protein; FOXP2_MOUSE; FOXP2_RAT; forkhead box P2; trinucleotide repeat containing 10; forkhead/winged-hel
Total $200.0
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  • NO.:SLA3154M
    React Species:Human, Mouse, Rat
    Immunogen Species:Rabbit
    Clonality:Recombinant
    Applications:WB, IHC-P, IHC-F, IF, ELISA, IP
    Gene name:FOXP2
    UniProt Entry:O15409
    NCBI Gene Entry:93986
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Product NameRecombinant Rabbit Anti-FOXP2 Monoclonal Antibody
Cat No.SLA3154M
AliasCAGH44; SPCH1; TNRC10; 2810043D05Rik; CAG-16; D0Kist7; RGD1559697; FOXP2_HUMAN; FOXP2; CAG repeat protein 44; Trinucleotide repeat-containing gene 10 protein; FOXP2_MOUSE; FOXP2_RAT; forkhead box P2; trinucleotide repeat containing 10; forkhead/winged-helix transcription factor; speech and language disorder 1; Forkhead box protein P2
Host SpeciesRabbit
IsotypeIgG
ClonalityMonoclonal
Clone No.11A4
React SpeciesHuman,Mouse,Rat
ApplicationsWB (1:500-2000)
IHC-P (1:50-200)
IHC-F (1:50-200)
IF (1:50-200)
ELISA (1:5000-10000)
IP (1:50-200)
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
Purificationaffinity purified by Protein A
Gene ID93986
Swiss-ProtO15409
Storage0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
BackgroundThis 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 isofor
AttentionThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.

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