Catalog No.
YHK38001
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Arg59-Ser332
Predicted molecular weight
33.32 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
Q9H9J2
Applications
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Form
Lyophilized
Storage buffer
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Reconstitution
Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping
In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternative Names
MRPL44, 39S ribosomal protein L44, mitochondrial, Mitochondrial large ribosomal subunit protein mL44, L44mt, MRP-L44
Note
For research use only.
Cloning and analysis of the nuclear genes for two mitochondrial ribosomal proteins in yeast., PMID:2693936
Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy., PMID:23315540
A metabolic phenotype based on mitochondrial ribosomal protein expression as a predictor of lymph node metastasis in papillary thyroid carcinoma., PMID:25590838
MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathy., PMID:25797485
A Role for the Mitochondrial Protein Mrpl44 in Maintaining OXPHOS Capacity., PMID:26221731
Mitochondrial ribosomal proteins involved in tellurite resistance in yeast Saccharomyces cerevisiae., PMID:30104660
Exploring rare and low-frequency variants in the Saguenay-Lac-Saint-Jean population identified genes associated with asthma and allergy traits., PMID:30206357
Genetic Basis of Severe Childhood-Onset Cardiomyopathies., PMID:30384889
LONP1 de novo dominant mutation causes mitochondrial encephalopathy with loss of LONP1 chaperone activity and excessive LONP1 proteolytic activity., PMID:31923470
Nuclear-encoded mitochondrial ribosomal proteins are required to initiate gastrulation., PMID:32376682
Expression analysis of mammalian mitochondrial ribosomal protein genes., PMID:32987154
Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial disease., PMID:33742325
Pathogenic variants in MRPL44 cause infantile cardiomyopathy due to a mitochondrial translation defect., PMID:34140213
Mitochondrial ribosomal protein genes connected with Alzheimer's and tellurite toxicity., PMID:35218961
Mitochondrial Neurodegenerative Diseases: Three Mitochondrial Ribosomal Proteins as Intermediate Stage in the Pathway That Associates Damaged Genes with Alzheimer's and Parkinson's., PMID:37508402
Importance of conserved hydrophobic pocket region in yeast mitoribosomal mL44 protein for mitotranslation and transcript preference., PMID:38950860
A novel likely pathogenic variant in the mitochondrial ribosomal protein L44 (MRPL44) associated with hypertrophic cardiomyopathy in Tunisian patients., PMID:40402202
For research use only. Not for human or drug use.
