PRX ELISA Kit for Human(Homo sapiens) | EIAab.comPRX ELISA Kit for Human(Homo sapiens)

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

PRX (Gene name),

Periaxin (Protein name ), PRAX_HUMAN from NCBI database.

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General Annotation

Antigen Annotation

Predicted Eptitope

Vaild Sequence

Related Databases

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Gene name:

PRX(KIAA1620);

Protein name:

Periaxin;

Alternative:

Organism:

Human (Homo sapiens).

General Annotation

Sub Unit:

Interacts with SCN10A. Found in a complex with SCN10A.

Function:

Seems to be required for maintenance of peripheral nerve myelin sheath. May have a role in axon-glial interactions, possibly by interacting with the cytoplasmic domains of integral membrane proteins such as myelin-associated glycoprotein in the periaxonal regions of the Schwann cell plasma membrane. May have a role in the early phases of myelin deposition.

Subcellular Location:

Isoform 2 Cytoplasm

Protein Attributes:

Sequence length:

1461

Sequence:

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1450:

1461:

ARMEGAQAAA | V

3D Structure:

N/A

Predicted Eptitope:

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Vaild Sequence:

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Related Databases

UniGene:

Hs.205457

MIM:

145900

SMR:

Q9BXM0

KEGG:

hsa:57716

STRING:

9606.ENSP00000326018

String:

Q9BXM0

Uniprot:

Q9BXM0

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ELISA Kit for Human Periaxin

Cat.:

E13230r

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Packing:

96T

ELISA Kit for Human Periaxin

Cat.:

E13230m

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MSDS:

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Packing:

96T

ELISA Kit for Human Periaxin

Cat.:

E13230h

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Manual:

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96T

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CLIA Kit for Human Periaxin

Cat.:

U13230h

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Manual:

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96T

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CLIA Kit for Human Periaxin

Cat.:

U13230m

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Packing:

96T

CLIA Kit for Human Periaxin

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Polyclonal Antibody for Human Periaxin

Monoclonal Antibody for Human Periaxin

Protein for Human Periaxin

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

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References

1.

"Periaxin mutations cause recessive Dejerine-Sottas neuropathy."
Boerkoel C.F. , Takashima H. , Stankiewicz P. , Garcia C.A. , Leber S.M. , Rhee-Morris L. , Lupski J.R.
Am. J. Hum. Genet.68:325-333(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: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 1 AND 2);VARIANTS THR-406; GLN-495; ALA-882; MET-921; GLU-935; ARG-1083; ARG-1132; LYS-1259; GLU-1359 DEL AND CYS-1411
2.

"Prediction of the coding sequences of unidentified human genes. XVIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro."
Nagase T. , Kikuno R. , Nakayama M. , Hirosawa M. , Ohara O.
DNA Res.7:273-281(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 [LARGE SCALE MRNA] (ISOFORM 3);VARIANT ALA-882
tissue: Brain.
3.

"The DNA sequence and biology of human chromosome 19."
Grimwood J. , Gordon L.A. , Olsen A.S. , Terry A. , Schmutz J. , Lamerdin J.E. , Hellsten U. , Goodstein D. , Couronne O. , Tran-Gyamfi M. , Aerts A. , Altherr M. , Ashworth L. , Bajorek E. , Black S. , Branscomb E. , Caenepeel S. , Carrano A.V. , more...
Nature428:529-535(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]
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] (ISOFORM 1);VARIANT ARG-1132
tissue: PNS.
5.

"A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease."
Guilbot A. , Williams A. , Ravise N. , Verny C. , Brice A. , Sherman D.L. , Brophy P.J. , LeGuern E. , Delague V. , Bareil C. , Megarbane A. , Claustres M.
Hum. Mol. Genet.10:415-421(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: DISEASE;TISSUE SPECIFICITY
6.

"Late-onset Charcot-Marie-Tooth disease 4F caused by periaxin gene mutation."
Tokunaga S. , Hashiguchi A. , Yoshimura A. , Maeda K. , Suzuki T. , Haruki H. , Nakamura T. , Okamoto Y. , Takashima H.
Neurogenetics13:359-365(2012) [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 CMT4F ASN-651

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