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Product Details
27472-1-AP
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit
/ IgG
Class
Polyclonal
Type
Antibody
Immunogen
PEX26 Fusion Protein Ag26529 (1-246 aa encoded by BC016280)
Conjugate
Form
Liquid
Concentration
0.33 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7.3, with 50% glycerol
Contains
0.02% sodium azide
Storage conditions
-20°C
Shipping conditions
Wet ice (domestic); Dry ice (international)
Product Specific Information
Immunogen sequence: MKSDSSTSA APLRGLGGPL RSSEPVRAVP ARAPAVDLLE EAADLLVVHL DFRAALETCE RAWQSLANHA VAEEPAGTSL EVKCSLCVVG IQALAEMDRW QEVLSWVLQY YQVPEKLPPK VLELCILLYS KMQEPGAVLD VVGAWLQDPA NQNLPEYGAL AEFHVQRVLL PLGCLSEAEE LVVGSAAFGE ERRLDVLQAI HTARQQQKQE HSGSEEAQKP NLEGSVSHKF LSLPMLVRQL WDSAVSH (1-246 aa encoded by BC016280)
Target Information
This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8. PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome, neonatal adrenoleukodystrophy, infantile Refsum disease, and classical rhizomelic chondrodysplasia punctata. Alternatively spliced transcript variants have been identified for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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Bioinformatics
Protein Aliases: FLJ20695; Peroxin-26; Peroxisome assembly protein 26; peroxisome biogenesis disorder, complementation group 8; peroxisome biogenesis disorder, complementation group A; peroxisome biogenesis factor 26
Gene Aliases: PBD7A; PBD7B; PEX26; PEX26M1T; Pex26pM1T
UniProt ID: (Human) Q7Z412
Entrez Gene ID: (Human) 55670
Performance Guarantee
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