anti-PEX7 (PEX7) Antikörper

Bezeichnung:: anti-Peroxisomal Biogenesis Factor 7 Antikörper (PEX7)

Auf www.antikoerper-online.de finden Sie aktuell 34 Peroxisomal Biogenesis Factor 7 (PEX7) Antikörper von 0 unterschiedlichen Herstellern. Insgesamt sind aktuell 45 PEX7 Produkte verfügbar.

Synonyme:: DDBDRAFT_0206295, DDBDRAFT_0233068, DDB_0206295, DDB_0233068, MmPEX7, PBD9B, Peroxin-7, pex7, PTS2R, RCDP1, RD, zgc:103552

Alle Antikörper anzeigen	Gen	GeneID	UniProt
Anti-Maus PEX7	PEX7	18634	P97865
Anti-Ratte PEX7	PEX7	308718
Anti-Human PEX7	PEX7	5191	O00628
Weitere Synonyme anzeigen

Verknüpfte Pathways mit anti-PEX7 Antikörper

Monocarboxylic Acid Catabolic Process

Weitere Produktkategorien zu PEX7 Antikörper

Am meisten referenzierte anti-PEX7 Antikörper

Human Polyclonal PEX7 Primary Antibody für WB - ABIN4891550 : Salcher, Hagenbuchner, Geiger, Seiter, Rainer, Kofler, Hermann, Kiechl-Kohlendorfer, Ausserlechner, Obexer: C10ORF10/DEPP, a transcriptional target of FOXO3, regulates ROS-sensitivity in human neuroblastoma. in Molecular cancer 2014 (PubMed)

Weitere Antikörper gegen PEX7 Interaktionspartner

Mouse (Murine) Peroxisomal Biogenesis Factor 7 (PEX7) Interaktionspartner

siRNA knockdown of PEX7 reduced iNOS (zeige NOS2 Antikörper) colocalization with the peroxisomal protein (zeige FNDC5 Antikörper) PMP70 (zeige ABCD3 Antikörper). Proteomic studies using MALDI-MS identified iNOS (zeige NOS2 Antikörper) association with the 50-kD ezrin (zeige EZR Antikörper) binding PDZ protein (zeige INADL Antikörper) (EBP50 (zeige SLC9A3R1 Antikörper)).
Our data established that peroxisomal processing protease Tysnd1 (zeige TYSND1 Antikörper) is necessary to mediate the physiological functions of PTS2-containing substrates.
Mutations in the Pex7 gene cause impaired neuronal migration and endochondral ossification.

Human Peroxisomal Biogenesis Factor 7 (PEX7) Interaktionspartner

This revealed a marked plasmalogen deficiency and a deficient fatty acid alpha-oxidation in the IHH (zeige IHH Antikörper) cells, due to a defect of PEX7, a cytosolic receptor protein required for peroxisomal import of a subset of peroxisomal proteins.
our data suggest that insertion of the trimeric PEX5 (zeige PEX5 Antikörper)-PEX7-PTS2 protein complex into the DTM is probably accompanied by conformational alterations in PEX5 (zeige PEX5 Antikörper) to allow release of the PTS2 protein into the organelle matrix
Mutation in the PEX7 Gene is associated with Rhizomelic Chondrodysplasia (zeige COL11A1 Antikörper) Punctata Type 1.
the sequential formation of a highly stable trimeric complex involving cargo protein, PEX7 and PEX5L (zeige PEX5L Antikörper) stabilizes cargo binding and is a prerequisite for PTS2-mediated peroxisomal import.
dysfunctional Pex7p, including mutants from RCDP patients, is degraded by a ubiquitin-dependent proteasomal pathway involving the CRL4A (Cullin4A-RING ubiquitin ligase) complex.
Export of peroxisomal PEX7 back into the cytosol requires export of PEX5 (zeige PEX5 Antikörper).
Structural requirements for interaction of peroxisomal targeting signal 2 and its receptor PEX7.
Mutations in PEX7 gene is associated with Rhizomelic chondrodysplasia (zeige COL11A1 Antikörper) punctata.
mutational spectrum in the PEX7 gene of 78 patients (including five pairs of sibs) clinically and biochemically diagnosed with RCDP type I
The residual activity of mutant Pex7 protein in rhizomelic chondrodysplasia (zeige COL11A1 Antikörper) punctata patients and reduced amounts of normal Pex7 are associated with milder and variant phenotypes.

PEX7 Antigen-Profil

Beschreibung des Gens

This gene encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in this gene cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD).

Alternative names and synonyms associated with PEX7

peroxisomal biogenesis factor 7 (PEX7) Antikörper
peroxisomal biogenesis factor 7 (pex7) Antikörper
WD40 repeat-containing protein (pex7) Antikörper
peroxisomal biogenesis factor 7 (Pex7) Antikörper

DDBDRAFT_0206295 Antikörper
DDBDRAFT_0233068 Antikörper
DDB_0206295 Antikörper
DDB_0233068 Antikörper
MmPEX7 Antikörper
PBD9B Antikörper
Peroxin-7 Antikörper
pex7 Antikörper
PTS2R Antikörper
RCDP1 Antikörper
RD Antikörper
zgc:103552 Antikörper

Bezeichner auf Proteinebene für PEX7

peroxisomal biogenesis factor 7 , peroxin 7 , peroxisome targeting signal type 2 receptor , peroxisomal targeting signal 2 receptor-like , PTS2 receptor , peroxin-7 , peroxisomal targeting signal 2 receptor , peroxisome biogenesis factor 7 , peroxisomal PTS2 receptor , peroxisome targeting signal 2 receptor

GENE ID	SPEZIES
463024	Pan troglodytes
548708	Xenopus (Silurana) tropicalis
705103	Macaca mulatta
8622229	Dictyostelium discoideum AX4
100218417	Taeniopygia guttata
100340758	Oryctolagus cuniculus
100406688	Callithrix jacchus
100454677	Pongo abelii
100596362	Nomascus leucogenys
18634	Mus musculus
308718	Rattus norvegicus
5191	Homo sapiens
541405	Danio rerio
421687	Gallus gallus
484000	Canis lupus familiaris
533077	Bos taurus
100736556	Cricetulus griseus

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Show all anti-Peroxisomal Biogenesis Factor 7 (PEX7) Antikörper with Pubmed References

Mouse (Murine) Peroxisomal Biogenesis Factor 7 (PEX7) Interaktionspartner

Human Peroxisomal Biogenesis Factor 7 (PEX7) Interaktionspartner

Beschreibung des Gens

Alternative names and synonyms associated with PEX7

Bezeichner auf Proteinebene für PEX7