ENAM ELISA Kit for Human(Homo sapiens) | EIAab.comENAM ELISA Kit for Human(Homo sapiens)

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

ENAM (Gene name),

Enamelin (Protein name ), ENAM_HUMAN from NCBI database.

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General Annotation

Antigen Annotation

Predicted Eptitope

Vaild Sequence

Related Databases

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Gene name:

ENAM;

Protein name:

Enamelin;

Alternative:

Organism:

Human (Homo sapiens).

General Annotation

Sub Unit:

N/A

Function:

Involved in the mineralization and structural organization of enamel. Involved in the extension of enamel during the secretory stage of dental enamel formation.

Subcellular Location:

Secreted extracellular space extracellular matrix

Protein Attributes:

Sequence length:

1142

Sequence:

50:

100:

150:

200:

250:

300:

350:

400:

450:

500:

550:

600:

650:

700:

750:

800:

850:

900:

950:

1000:

1050:

1100:

1142:

TEEQFKSINV | DPLDADEHSP | FEFLQRGTNV | QDQVQDCLLL | QA

3D Structure:

N/A

Predicted Eptitope:

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Vaild Sequence:

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Related Databases

MIM:

104500

Pfam:

PF15362

KEGG:

hsa:10117

UniGene:

Hs.667018

STRING:

9606.ENSP00000379383

String:

Q9NRM1

Uniprot:

Q9NRM1

FOR

ELISA Kit for Human Enamelin

CLIA Kit for Human Enamelin

Polyclonal Antibody for Human Enamelin

Monoclonal Antibody for Human Enamelin

Protein for Human Enamelin

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.

"Dietary change and adaptive evolution of enamelin in humans and among primates."
Kelley J.L. , Swanson W.J.
Genetics178:1595-1603(2008) [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];VARIANTS THR-648 AND GLN-763
2.

"cDNA sequence of human enamelin."
Hu C.-C. , Qian Q. , Zhang C. , Fukae M. , Uchida T. , Simmer J.P.
Submitted (1999-02) 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 [MRNA]
3.

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]
4.

"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res.14:2121-2127(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 MRNA]
5.

"Enamelin maps to human chromosome 4q21 within the autosomal dominant amelogenesis imperfecta locus."
Dong J. , Gu T.T. , Simmons D. , MacDougall M.
Eur. J. Oral Sci.108:353-358(2000) [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] OF 1014-1142
6.

"Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta."
Rajpar M.H. , Harley K. , Laing C. , Davies R.M. , Dixon M.J.
Hum. Mol. Genet.10:1673-1677(2001) [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: INVOLVEMENT IN AI1B
7.

"A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2)."
Mardh C.K. , Backman B. , Holmgren G. , Hu J.C. , Simmer J.P. , Forsman-Semb K.
Hum. Mol. Genet.11:1069-1074(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: INVOLVEMENT IN AI1B
8.

"Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects."
Hart T.C. , Hart P.S. , Gorry M.C. , Michalec M.D. , Ryu O.H. , Uygur C. , Ozdemir D. , Firatli S. , Aren G. , Firatli E.
J. Med. Genet.40:900-906(2003) [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: INVOLVEMENT IN AI1C

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