The C4orf3 gene in mice encodes a protein with a predicted role in calcium ion regulation. While the full-length human homolog (ARLN) spans 199 amino acids, the recombinant mouse version is a shorter isoform (1–65 aa) focused on conserved functional domains .
The protein is expressed in E. coli with an N-terminal His tag, followed by purification via nickel affinity chromatography. Key specifications include:
Parameter | Value |
---|---|
Purity | >90% (SDS-PAGE validation) |
Form | Lyophilized powder |
Storage Buffer | Tris/PBS-based buffer with 6% trehalose, pH 8.0 |
Reconstitution | 0.1–1.0 mg/mL in sterile water; glycerol (5–50%) recommended for storage |
Storage | -20°C/-80°C; avoid freeze-thaw cycles |
Application | Use Case |
---|---|
Cell Culture | Studying ER calcium dynamics and SERCA regulation |
In Vitro Studies | ELISA assays, protein-protein interaction mapping |
Drug Discovery | Screening inhibitors of calcium homeostasis pathways |
The full-length C4orf3 homolog (ARLN) interacts with SERCA to modulate calcium uptake in the endoplasmic reticulum . While the recombinant mouse isoform lacks the transmembrane domain, it may retain partial functionality for studying:
SERCA inhibition: Binding to the inhibitory groove of SERCA.
Hepatitis C Virus (HCV) Pathogenesis: The human homolog is transactivated by HCV F protein (HCVFTP1) .
Feature | Mouse (Q99M08) | Rat (Q498U0) |
---|---|---|
Sequence Length | 65 aa | 65 aa |
AA Sequence | MEVSQAASGTDGVRERRGSFEAGRRNQDEAPQSGMNGLPKHSYWLDLWLFILFDLALFVF VYLLP | MEVGQAASGTDGVRERRGSSAARRRSQDEPVQSGMNGIPKHSYWLDLWLFILFDLALFIF VYLLP |
Expression System | E. coli | E. coli |
Purity | >90% | >90% |
Calcium Homeostasis Studies:
Investigating SERCA activity modulation in neuronal or liver cells.
Assessing interactions with calcium-binding proteins (e.g., calmodulin).
Viral Pathogenesis:
Modeling HCV infection mechanisms using the recombinant protein.
Structural Biology:
Crystallization for 3D structure determination of the N-terminal domain.
Functional Truncation: The recombinant isoform lacks the C-terminal transmembrane domain, limiting membrane localization studies.
Species-Specific Effects: Mouse and human homologs may differ in SERCA binding efficiency.