Full Product Name
FOXI1 (Forkhead Box I1, FKHL10, Forkhead-Related Transcription Factor 6, FREAC6, HNF-3 Forkhead Homolog 3, HFH3)
Product Synonym Names
Anti -FOXI1 (Forkhead Box I1, FKHL10, Forkhead-Related Transcription Factor 6, FREAC6, HNF-3 Forkhead Homolog 3, HFH3)
Product Gene Name
anti-FOXI1 antibody
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Immunogen Sequence
MSSFDLPAPS PPRCSPQFPS IGQEPPEMNL YYENFFHPQG VPSPQRPSFE GGGEYGATPN PYLWFNGPTM TPPPYLPGPN ASPFLPQAYG VQRPLLPSVS GLGGSDLGWL PIPSQEELMK LVRPPYSYSA LIAMAIHGAP DKRLTLSQIY QYVADNFPFY NKSKAGWQNS IRHNLSLNDC FKKVPRDEDD PAYVSGGSPT SHPLVTPGLS PEPSDKTGQN SLTFNSFSPL TNLSNHSGGG DWANPMPTNM LSYGGSVLSQ FSPHFYNSVN TSGVLYPREG TEV
Chromosome Location
Chromosome: 5; NC_000005.9 (169532917..169536729). Location: 5q34
3D Structure
ModBase 3D Structure for Q12951
Specificity
Recognizes human FOXI1.
Purity/Purification
Affinity Purified
Purified by Protein A affinity chromatography.
Form/Format
Supplied as a liquid in PBS, pH 7.2.
Immunogen
Full length human FOXI1, aa1-283 (NP_658982.1).
Preparation and Storage
May be stored at 4 degree C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degree C. Aliquots are stable for at least 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Other Notes
Small volumes of anti-FOXI1 antibody 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.
Related Product Information for
anti-FOXI1 antibody
This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it is possible that this gene plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis. Mutations in this gene may be associated with the common cavity phenotype. Two transcript variants encoding different isoforms have been found for this gene.
Product Categories/Family for anti-FOXI1 antibody
Antibodies; Abs to Transcription Factors
Applications Tested/Suitable for anti-FOXI1 antibody
Western Blot (WB), Immunofluorescence (IF)
Application Notes for anti-FOXI1 antibody
Suitable for use in Immunofluorescence and Western Blot.
Dilution: Immunofluorescence: 10ug/ml
NCBI/Uniprot data below describe general gene information for FOXI1. It may not necessarily be applicable to this product.
NCBI Accession #
NP_658982.1
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NCBI GenBank Nucleotide #
NM_144769.2
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UniProt Primary Accession #
Q12951
[Other Products]
UniProt Secondary Accession #
Q14518; Q66SR7; Q8N6L8[Other Products]
UniProt Related Accession #
Q12951[Other Products]
Molecular Weight
40,973 Da[Similar Products]
NCBI Official Full Name
forkhead box protein I1 isoform b
NCBI Official Synonym Full Names
forkhead box I1
NCBI Official Symbol
FOXI1 [Similar Products]
NCBI Official Synonym Symbols
HFH3; FKH10; HFH-3; FKHL10; FREAC6; FREAC-6
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NCBI Protein Information
forkhead box protein I1; forkhead-like 10; HNF-3/fork-head homolog 3; HNF-3/fork-head homolog-3; forkhead-related activator 6; forkhead-related protein FKHL10; forkhead-related transcription factor 6; hepatocyte nuclear factor 3 forkhead homolog 3
UniProt Protein Name
Forkhead box protein I1
UniProt Synonym Protein Names
Forkhead-related protein FKHL10; Forkhead-related transcription factor 6; FREAC-6; Hepatocyte nuclear factor 3 forkhead homolog 3
Protein Family
Forkhead box protein
UniProt Gene Name
FOXI1 [Similar Products]
UniProt Synonym Gene Names
FKHL10; FREAC6; FREAC-6; HFH-3 [Similar Products]
UniProt Entry Name
FOXI1_HUMAN
NCBI Summary for FOXI1
This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it is possible that this gene plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis. Mutations in this gene may be associated with the common cavity phenotype. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
UniProt Comments for FOXI1
FOXI1: Transcriptional activator required for the development of normal hearing, sense of balance and kidney function. Required for the expression of SLC26A4/PDS, JAG1 and COCH in a subset of epithelial cells and the development of the endolymphatic system in the inner ear. Also required for the expression of SLC4A1/AE1, SLC4A9/AE4, ATP6V1B1 and the differentiation of intercalated cells in the epithelium of distal renal tubules. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: DNA-binding
Chromosomal Location of Human Ortholog: 5q34
Cellular Component: nucleus
Molecular Function: sequence-specific DNA binding; transcription factor activity; DNA bending activity
Biological Process: embryonic development; inner ear morphogenesis; transcription, DNA-dependent; positive regulation of transcription from RNA polymerase II promoter
Disease: Pendred Syndrome; Deafness, Autosomal Recessive 4, With Enlarged Vestibular Aqueduct
Research Articles on FOXI1
1. We found no evidence for a significant association between mutations of KCNJ10 and FOXI1 with SLC26A4 in Pendred syndrome/enlarged vestibular aqueducts.
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