PEX13 ELISA Kit for Human(Homo sapiens) | EIAab.comPEX13 ELISA Kit for Human(Homo sapiens)

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PEX13 (Gene name),

Peroxisomal membrane protein PEX13 (Protein name ), PEX13_HUMAN from NCBI database.

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General Annotation

Antigen Annotation

Predicted Eptitope

Vaild Sequence

Related Databases

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Gene name:

PEX13;

Protein name:

Peroxisomal membrane protein PEX13;

Alternative:

Peroxin-13;

Organism:

Human (Homo sapiens).

General Annotation

Sub Unit:

Interacts with PEX19.

Function:

Component of the peroxisomal translocation machinery with PEX14 and PEX17. Functions as a docking factor for the predominantly cytoplasmic PTS1 receptor (PAS10/PEX5). Involved in the import of PTS1 and PTS2 proteins.

Subcellular Location:

Peroxisome membrane Single-pass membrane protein

Protein Attributes:

Sequence length:

403

Sequence:

50:

100:

150:

200:

250:

300:

350:

400:

403:

QDL

3D Structure:

N/A

Predicted Eptitope:

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Vaild Sequence:

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Related Databases

KEGG:

hsa:5194

String:

Q92968

MIM:

202370

MIM:

601789

STRING:

9606.ENSP00000295030

UniGene:

Hs.161377

SMR:

Q92968

Pfam:

PF04088

Uniprot:

Q92968

FOR

ELISA Kit for Human Peroxisomal membrane protein PEX13

CLIA Kit for Human Peroxisomal membrane protein PEX13

Polyclonal Antibody for Human Peroxisomal membrane protein PEX13

Monoclonal Antibody for Human Peroxisomal membrane protein PEX13

Protein for Human Peroxisomal membrane protein PEX13

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.

"Identification of a human PTS1 receptor docking protein directly required for peroxisomal protein import."
Fransen M. , Terlecky S.R. , Subramani S.
Proc. Natl. Acad. Sci. U.S.A.95:8087-8092(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: NUCLEOTIDE SEQUENCE [MRNA]
2.

"Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants."
Toyama R. , Mukai S. , Itagaki A. , Tamura S. , Shimozawa N. , Suzuki Y. , Kondo N. , Wanders R.J. , Fujiki Y.
Hum. Mol. Genet.8:1673-1681(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 [MRNA]
3.

"Complete sequencing and characterization of 21,243 full-length human cDNAs."
Ota T. , Suzuki Y. , Nishikawa T. , Otsuki T. , Sugiyama T. , Irie R. , Wakamatsu A. , Hayashi K. , Sato H. , Nagai K. , Kimura K. , Makita H. , Sekine M. , Obayashi M. , Nishi T. , Shibahara T. , Tanaka T. , Ishii S. , more...
Nat. Genet.36:40-45(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]
tissue: Trachea.
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 (2005-09) 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]
tissue: Liver.
6.

"Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptor."
Gould S.J. , Kalish J.E. , Morrell J.C. , Bjoerkman J. , Urquhart A.J. , Crane D.I.
J. Cell Biol.135:85-95(1996) [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 40-403
7.

"PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis."
Sacksteder K.A. , Jones J.M. , South S.T. , Li X. , Liu Y. , Gould S.J.
J. Cell Biol.148:931-944(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: INTERACTION WITH PEX19
8.

"Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences."
Fransen M. , Wylin T. , Brees C. , Mannaerts G.P. , Van Veldhoven P.P.
Mol. Cell. Biol.21:4413-4424(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: INTERACTION WITH PEX19;SUBCELLULAR LOCATION
9.

"Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations."
Al-Dirbashi O.Y. , Shaheen R. , Al-Sayed M. , Al-Dosari M. , Makhseed N. , Abu Safieh L. , Santa T. , Meyer B.F. , Shimozawa N. , Alkuraya F.S.
Am. J. Med. Genet. A149:1219-1223(2009) [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 PBD11A
10.

"PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders."
Liu Y. , Bjoerkman J. , Urquhart A. , Wanders R.J.A. , Crane D.I. , Gould S.J.
Am. J. Hum. Genet.65:621-634(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: VARIANT PBD11B THR-326
11.

"Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders."
Shimozawa N. , Suzuki Y. , Zhang Z. , Imamura A. , Toyama R. , Mukai S. , Fujiki Y. , Tsukamoto T. , Osumi T. , Orii T. , Wanders R.J.A. , Kondo N.
Hum. Mol. Genet.8:1077-1083(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: INVOLVEMENT IN PBD11A;VARIANT PBD11B THR-326

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