PEX19 (NM_002857) Human Mass Spec Standard

CAT#: PH301756

PEX19 MS Standard C13 and N15-labeled recombinant protein (NP_002848)



  View other "PEX19" proteins (4)

Need it in bulk or customized?
Get a free quote

CNY 19,520.00


货期*
4周

规格
    • 10 ug

Product images

经常一起买 (2)
Transient overexpression lysate of peroxisomal biogenesis factor 19 (PEX19), transcript variant 1
    • 100 ug

CNY 3,080.00


Rabbit Polyclonal antibody to PEX19 (peroxisomal biogenesis factor 19)
    • 100 ul

CNY 6,281.00

Specifications

Product Data
Description PEX19 MS Standard C13 and N15-labeled recombinant protein (NP_002848)
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC201756
Predicted MW 32.8 kDa
Protein Sequence
Tag C-Myc/DDK
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
Reference Data
RefSeq NP_002848
RefSeq Size 3722
RefSeq ORF 897
Synonyms D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF; PXMP1
Locus ID 5824
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
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Documents

Other Versions

Customer Reviews 
Loading...