FOXE1 ELISA Kit for Human(Homo sapiens) | EIAab.comFOXE1 ELISA Kit for Human(Homo sapiens)

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Index > Protein center > FOXE1(Gene name) > Human

FOXE1 (Gene name),

Forkhead box protein E1 (Protein name ), FOXE1_HUMAN from NCBI database.

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General Annotation

Antigen Annotation

Predicted Eptitope

Vaild Sequence

Related Databases

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Gene name:

FOXE1(FKHL15;FOXE2;TITF2;TTF2);

Protein name:

Forkhead box protein E1;

Alternative:

Forkhead-related protein FKHL15;Forkhead box protein E2;HNF-3/fork head-like protein 5(HFKL5);HFKH4;Thyroid transcription factor 2(TTF-2);

Organism:

Human (Homo sapiens).

General Annotation

Sub Unit:

N/A

Function:

Probable transcription factor. Could be involved in thyroid gland organogenesis.

Subcellular Location:

Nucleus

Protein Attributes:

Sequence length:

373

Sequence:

50:

100:

150:

200:

250:

300:

350:

373:

AGAYHARHAA | AYPGGIDRFV | SAM

3D Structure:

N/A

Predicted Eptitope:

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Vaild Sequence:

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Related Databases

STRING:

9606.ENSP00000364265

SMR:

O00358

MIM:

241850

UniGene:

Hs.159234

String:

O00358

Pfam:

PF00250

KEGG:

hsa:2304

Uniprot:

O00358

FOR

ELISA Kit for Human Forkhead box protein E1

CLIA Kit for Human Forkhead box protein E1

Polyclonal Antibody for Human Forkhead box protein E1

Monoclonal Antibody for Human Forkhead box protein E1

Protein for Human Forkhead box protein E1

R&D Technical Data

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

Precision

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

Recovery

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

Linearity

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

References

1.

"The novel human HNF-3/fork head-like 5 gene: chromosomal localization and expression pattern."
Wiese S. , Emmerich D. , Schroeder B. , Murphy D.B. , Grzeschik K.H. , Van Kessel A.G. , Thies U.
DNA Cell Biol.16:165-171(1997) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: PRELIMINARY NUCLEOTIDE SEQUENCE [MRNA]
tissue: Fetal brain.
2.

"FKHL15, a new human member of the forkhead gene family located on chromosome 9q22."
Chadwick B.P. , Obermayr F. , Frischauf A.-M.
Genomics41:390-396(1997) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [MRNA];POLYMORPHISM OF POLY-ALA REGION
tissue: Keratinocyte.
3.

"Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2)."
Macchia P.E. , Mattei M.-G. , Lapi P. , Fenzi G. , Di Lauro R.
Biochimie81:433-440(1999) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA];POLYMORPHISM
4.

"DNA sequence and analysis of human chromosome 9."
Humphray S.J. , Oliver K. , Hunt A.R. , Plumb R.W. , Loveland J.E. , Howe K.L. , Andrews T.D. , Searle S. , Hunt S.E. , Scott C.E. , Jones M.C. , Ainscough R. , Almeida J.P. , Ambrose K.D. , Ashwell R.I.S. , Babbage A.K. , Babbage S. , Bagguley C.L. , more...
Nature429:369-374(2004) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]
5.

Mural R.J. , Istrail S. , Sutton G.G. , Florea L. , Halpern A.L. , Mobarry C.M. , Lippert R. , Walenz B. , Shatkay H. , Dew I. , Miller J.R. , Flanigan M.J. , Edwards N.J. , Bolanos R. , Fasulo D. , Halldorsson B.V. , Hannenhalli S. , Turner R. , more...
Submitted (2005-07) to the EMBL/GenBank/DDBJ databases

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]
6.

"Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia."
Clifton-Bligh R.J. , Wentworth J.M. , Heinz P. , Crisp M.S. , John R. , Lazarus J.H. , Ludgate M. , Chatterjee V.K.
Nat. Genet.19:399-401(1998) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT BLS VAL-65
7.

"A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate."
Castanet M. , Park S.M. , Smith A. , Bost M. , Leger J. , Lyonnet S. , Pelet A. , Czernichow P. , Chatterjee K. , Polak M.
Hum. Mol. Genet.11:2051-2059(2002) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT BLS ASN-57
8.

"A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis."
Baris I. , Arisoy A.E. , Smith A. , Agostini M. , Mitchell C.S. , Park S.M. , Halefoglu A.M. , Zengin E. , Chatterjee V.K. , Battaloglu E.
J. Clin. Endocrinol. Metab.91:4183-4187(2006) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT CONGENITAL HYPOTHYROIDISM CYS-102;CHARACTERIZATION OF VARIANT CONGENITAL HYPOTHYROIDISM CYS-102

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