CRPPA (NM_001101417) Human Recombinant Protein
Selected Variant
PH33552M5
Size: 20 µg
Product Specifications
Background
This gene encodes a 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase-like protein. Mutations in this gene are the cause of Walker-Warburg syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2012]
Overview
Recombinant protein of human notch1-induced protein (LOC729920), transcript variant 2
Synonyms
HISPD; ISPD; LGMDR20; MDDGA7; MDDGC7; Nip
Gene ID
729920
UniProt
A4D126, A0A140VJM1
Accession Number mRNA
NM_001101417
Chromosomal Location
7p21.2
Expression System
HEK293T
Tag
C-Myc/DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Molecular Weight
44.2 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
CRPPA
Species
Human
Protein ID
NP_001094887
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/729920
Uniprot URL
https://www.uniprot.org/uniprot/A4D126
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_001101417
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_001094887
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