ARL13B (NM_144996) Human Recombinant Protein
Product Specifications
Background
This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]
Synonyms
ARL2L1; JBTS8
Gene ID
200894
UniProt
Q3SXY8
Accession Number mRNA
NM_144996
Chromosomal Location
3q11.1-q11.2
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
36.6 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
ARL13B
Species
Human
Protein ID
NP_659433
Overview
Recombinant protein of human ADP-ribosylation factor-like 13B (ARL13B), transcript variant 2
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/200894
Uniprot URL
https://www.uniprot.org/uniprot/Q3SXY8
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_144996
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_659433
Curated Selection
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