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RTN4IP1 (NM_032730) Human Recombinant Protein

Product Specifications

Background

This gene encodes a mitochondrial protein that interacts with reticulon 4, which is a potent inhibitor of regeneration following spinal cord injury. This interaction may be important for reticulon-induced inhibition of neurite growth. Mutations in this gene can cause optic atrophy 10, with or without ataxia, cognitive disability, and seizures. There is a pseudogene for this gene on chromosome 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

Overview

Recombinant protein of human reticulon 4 interacting protein 1 (RTN4IP1), nuclear gene encoding mitochondrial protein

Synonyms

NIMP; OPA10

Gene ID

84816

UniProt

Q8WWV3

Accession Number mRNA

NM_032730

Chromosomal Location

6q21

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

Function

Druggable Genome

Molecular Weight

38.9 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

RTN4IP1

Species

Human

Protein ID

NP_116119

Gene ID URL

https://www.ncbi.nlm.nih.gov/gene/84816

Uniprot URL

https://www.uniprot.org/uniprot/Q8WWV3

Accession Number mRNA URL

https://www.ncbi.nlm.nih.gov/nuccore/NM_032730

Protein ID Link

https://www.ncbi.nlm.nih.gov/nuccore/NP_116119

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