PEX19 (NM_002857) Human Mass Spec Standard

SKU
PH301756
PEX19 MS Standard C13 and N15-labeled recombinant protein (NP_002848)
  $3,360.00
3 Weeks*
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Specifications
Specifications
Product Data
Tag C-Myc/DDK
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC201756
Predicted MW 32.8 kDa
Protein Sequence
Protein Sequence
>RC201756 protein sequence
Red=Cloning site Green=Tags(s)

MAAAEEGCSVGAEADRELEELLESALDDFDKAKPSPAPPSTTTAPDASGPQKRSPGDTAKDALFASQEKF
FQELFDSELASQATAEFEKAMKELAEEEPHLVEQFQKLSEAAGRVGSDMTSQQEFTSCLKETLSGLAKNA
TDLQNSSMSEEELTKAMEGLGMDEGDGEGNILPIMQSIMQNLLSKDVLYPSLKEITEKYPEWLQSHRESL
PPEQFEKYQEQHSVMCKICEQFEAETPTDSETTQKARFEMVLDLMQQLQDLGHPPKELAGEMPPGLNFDL
DALNLSGPPGASGEQCLIM

TRTRPLEQKLISEEDLAANDILDYKDDDDKV
Purity > 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration >0.05 µg/µL as determined by microplate BCA method
Labeling Method Labeled with U- 13C6, 15N4-L-Arginine and U- 13C6, 15N2-L-Lysine
Buffer 25 mM Tris-HCl, 100 mM glycine, pH 7.3
Storage Store at -80°C. Avoid repeated freeze-thaw cycles.
Stability Stable for 3 months from receipt of products under proper storage and handling conditions.
Shipping Dry Ice
Reference Data
RefSeq NP_002848
RefSeq Size 3722
RefSeq ORF 897
Synonyms D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF; PXMP1
Locus ID 5824
UniProt ID P40855
Cytogenetics 1q23.2
Summary This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). 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. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some 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 Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. provided by RefSeq, Aug 2010
Protein Families Druggable Genome
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Documents
Resources
Other "PEX19" proteins (4)
SKU Description Size Price
LC419085 Lyophilized PEX19 HEK293T cell transient overexpression lysate (as WB positive control) 20 ug
$206.00
LY419085 Transient overexpression lysate of peroxisomal biogenesis factor 19 (PEX19), transcript variant 1 (as WB positive control) 100 ug
$436.00
TP301756 Recombinant protein of human peroxisomal biogenesis factor 19 (PEX19), transcript variant 1, 20 µg 20 ug
$867.00
TP325241 Purified recombinant protein of Homo sapiens peroxisomal biogenesis factor 19 (PEX19), transcript variant 2, 20 µg 20 ug
$867.00

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