VSX2 ELISA Kit for Human(Homo sapiens) | EIAab.comVSX2 ELISA Kit for Human(Homo sapiens)

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Index > Protein center > VSX2(Gene name) > Human

VSX2 (Gene name),

Visual system homeobox 2 (Protein name ), VSX2_HUMAN from NCBI database.

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General Annotation

Antigen Annotation

Predicted Eptitope

Vaild Sequence

Related Databases

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Gene name:

VSX2(CHX10;HOX10);

Protein name:

Visual system homeobox 2;

Alternative:

Homeobox protein CHX10;Ceh-10 homeodomain-containing homolog;

Organism:

Human (Homo sapiens).

General Annotation

Sub Unit:

N/A

Function:

Plays a significant role in the specification and morphogenesis of the sensory retina. May also participate in the development of the cells of the inner nuclear layer, particularly bipolar cells.

Subcellular Location:

Nucleus

Protein Attributes:

Sequence length:

361

Sequence:

50:

100:

150:

200:

250:

300:

350:

361:

RLSPPQLEDM | A

3D Structure:

N/A

Predicted Eptitope:

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Vaild Sequence:

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Related Databases

SMR:

P58304

KEGG:

hsa:338917

MIM:

142993

String:

P58304

STRING:

9606.ENSP00000261980

UniGene:

Hs.449771

Pfam:

PF00046

Uniprot:

P58304

FOR

ELISA Kit for Human Visual system homeobox 2

CLIA Kit for Human Visual system homeobox 2

Polyclonal Antibody for Human Visual system homeobox 2

Monoclonal Antibody for Human Visual system homeobox 2

Protein for Human Visual system homeobox 2

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.

"Human microphthalmia associated with mutations in the retinal homeobox gene CHX10."
Percin E.F. , Ploder L.A. , Yu J.J. , Arici K. , Horsford D.J. , Rutherford A. , Bapat B. , Cox D.W. , Duncan A.M.V. , Kalnins V.I. , Kocak-Altintas A. , Sowden J.C. , Traboulsi E. , Sarfarazi M. , McInnes R.R.
Nat. Genet.25:397-401(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 [GENOMIC DNA];VARIANTS MCOPCTI GLN-200 AND PRO-200
2.

"Cloning and characterization of human CHX10 (Ceh-10 homeodomain containing homolog) gene."
Shan Y.X. , Yu L.
Submitted (2003-07) 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 [MRNA]
3.

"The DNA sequence and analysis of human chromosome 14."
Heilig R. , Eckenberg R. , Petit J.-L. , Fonknechten N. , Da Silva C. , Cattolico L. , Levy M. , Barbe V. , De Berardinis V. , Ureta-Vidal A. , Pelletier E. , Vico V. , Anthouard V. , Rowen L. , Madan A. , Qin S. , Sun H. , Du H. , more...
Nature421:601-607(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: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]
4.

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]
5.

"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]
6.

"CHX10 mutations cause non-syndromic microphthalmia/ anophthalmia in Arab and Jewish kindreds."
Bar-Yosef U. , Abuelaish I. , Harel T. , Hendler N. , Ofir R. , Birk O.S.
Hum. Genet.115:302-309(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: INVOLVEMENT IN MCOPCB3;VARIANT MCOP2 TRP-227
7.

"VSX2 mutations in autosomal recessive microphthalmia."
Reis L.M. , Khan A. , Kariminejad A. , Ebadi F. , Tyler R.C. , Semina E.V.
Mol. Vis.17:2527-2532(2011) [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 MCOP2 ALA-223

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