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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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