Name: Anti-PEX5 Antibody (CAB12493)
Brand: Cell Biology Antibodies 3
SKU: CAB12493
Availability: OutOfStock

Antibody Name:	Anti-PEX5 Antibody
Antibody SKU:	CAB12493
Antibody Size:	20uL, 50uL, 100uL
Application:	WB
Reactivity:	Human, Mouse
Host Species:	Rabbit
Immunogen:	Recombinant fusion protein containing a sequence corresponding to amino acids 364-631 of human PEX5 (NP_000310.2).

Application:	WB
Recommended Dilution:	WB 1:500 - 1:2000
Reactivity:	Human, Mouse
Positive Samples:	U-251MG, HepG2, 293T, HeLa, Mouse brain, Mouse kidney, Mouse liver

Immunogen:	Recombinant fusion protein containing a sequence corresponding to amino acids 364-631 of human PEX5 (NP_000310.2).
Purification Method:	Affinity purification
Storage Buffer:	Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Isotype:	IgG
Sequence:	WQYL GTTQ AENE QELL AISA LRRC LELK PDNQ TALM ALAV SFTN ESLQ RQAC ETLR DWLR YTPA YAHL VTPA EEGA GGAG LGPS KRIL GSLL SDSL FLEV KELF LAAV RLDP TSID PDVQ CGLG VLFN LSGE YDKA VDCF TAAL SVRP NDYL LWNK LGAT LANG NQSE EAVA AYRR ALEL QPGY IRSR YNLG ISCI NLGA HREA VEHF LEAL NMQR KSRG PRGE GGAM SENI WSTL RLAL SMLG QSDA YGAA DARD LSTL LTMF GLPQ
Gene ID:	5830
Uniprot:	P50542
Cellular Location:	Cytoplasm, Peripheral membrane protein, Peroxisome membrane
Calculated MW:	66kDa/69kDa/70kDa/72kDa
Observed MW:	71kDa

Synonyms:

PEX5, PBD2A, PBD2B, PTS1-BP, PTS1R, PXR1, RCDP5

Background:

The product of this gene binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 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 are a cause of neonatal adrenoleukodystrophy (NALD), a cause of Zellweger syndrome (ZWS) as well as may be a cause of infantile Refsum disease (IRD). Alternatively spliced transcript variants encoding different isoforms have been identified.

UniProt Protein Function:	PEX5: Binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import. Defects in PEX5 are a cause of adrenoleukodystrophy neonatal (NALD). NALD is a peroxisome biogenesis disorder (PBD) characterized by the accumulation of very long- chain fatty acids, adrenal insufficiency and mental retardation. Inheritance is autosomal recessive. Defects in PEX5 are a cause of Zellweger syndrome (ZWS). ZWS is a fatal peroxisome biogenesis disorder characterized by dysmorphic facial features, hepatomegaly, ocular abnormalities, renal cysts, hearing impairment, profound psychomotor retardation, severe hypotonia and neonatal seizures. Death occurs within the first year of life. Defects in PEX5 may be a cause of infantile Refsum disease (IRD). IRD is a mild peroxisome biogenesis disorder (PBD). Clinical features include early onset, mental retardation, minor facial dysmorphism, retinopathy, sensorineural hearing deficit, hepatomegaly, osteoporosis, failure to thrive, and hypocholesterolemia. The biochemical abnormalities include accumulation of phytanic acid, very long chain fatty acids (VLCFA), di- and trihydroxycholestanoic acid and pipecolic acid. Belongs to the peroxisomal targeting signal receptor family. 4 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:	Protein type:Membrane protein, integral; Receptor, protein translocating Chromosomal Location of Human Ortholog: 12p13.31 Cellular Component: cytoplasm; cytosol; Golgi apparatus; membrane; peroxisomal membrane; peroxisome; protein complex Molecular Function:enzyme binding; peroxisome matrix targeting signal-1 binding; peroxisome targeting sequence binding; protein binding; protein N-terminus binding; small GTPase binding Biological Process: protein import into peroxisome matrix; protein import into peroxisome matrix, docking; protein import into peroxisome membrane Disease: Peroxisome Biogenesis Disorder 2a (zellweger); Peroxisome Biogenesis Disorder 2b; Rhizomelic Chondrodysplasia Punctata, Type 5
NCBI Summary:	The product of this gene binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 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 are a cause of neonatal adrenoleukodystrophy (NALD), a cause of Zellweger syndrome (ZWS) as well as may be a cause of infantile Refsum disease (IRD). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]
UniProt Code:	P50542
NCBI GenInfo Identifier:	119364633
NCBI Gene ID:	5830
NCBI Accession:	P50542.3
UniProt Secondary Accession:	P50542,Q15115, Q15266, Q96FN7, A8K891, B4DZ45, B7ZAD5 D3DUT8,
UniProt Related Accession:	P50542
Molecular Weight:	71kDa
NCBI Full Name:	Peroxisomal targeting signal 1 receptor
NCBI Synonym Full Names:	peroxisomal biogenesis factor 5
NCBI Official Symbol:	PEX5
NCBI Official Synonym Symbols:	PXR1; PBD2A; PBD2B; PTS1R; RCDP5; PTS1-BP
NCBI Protein Information:	peroxisomal biogenesis factor 5
UniProt Protein Name:	Peroxisomal targeting signal 1 receptor
UniProt Synonym Protein Names:	PTS1-BP; Peroxin-5; Peroxisomal C-terminal targeting signal import receptor; Peroxisome receptor 1
Protein Family:	PEX5-related protein
UniProt Gene Name:	PEX5

Western blot analysis of extracts of various cell lines, using PEX5 antibody (CAB12493) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Exposure time: 10s.

Antibodies

Anti-PEX5 Antibody (CAB5780)

PEX5 Antibody (PACO03050)

PEX5 Antibody (PACO11177)

Secondary Antibody

Anti-HRP Goat Anti-Rabbit IgG (H+L) Antibody (CABS014)