Catalog No.
YHA60901
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Arg65-Lys461
Predicted molecular weight
48.17 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
O43242
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
26S proteasome regulatory subunit S3, 26S proteasome regulatory subunit RPN3, Proteasome subunit p58, 26S proteasome non-ATPase regulatory subunit 3, PSMD3
Discovering new hub genes of dilated cardiomyopathy., PMID:40074718
Pluripotency factor Tex10 finetunes Wnt signaling for spermatogenesis and primordial germ cell development., PMID:39988597
Ubiquitination, SUMOylation, and NEDDylation related genes serve as prognostic and therapeutic biomarkers for oral squamous cell carcinoma., PMID:38234119
PSMD3-ILF3 signaling cascade drives lung cancer cell proliferation and migration., PMID:37337223
PSMD3 gene mutations cause pathological myopia., PMID:36948574
Interplay between hereditary and acquired factors determines the neutrophil counts in older individuals., PMID:36930802
19S Proteasome Subunits as Oncogenes and Prognostic Biomarkers in FLT3-Mutated Acute Myeloid Leukemia (AML)., PMID:36498916
Candidate genes for infertility: an in-silico study based on cytogenetic analysis., PMID:35918717
Proteomics Analysis of Aqueous Humor and Rejected Graft in Pig-to-Non-Human Primate Corneal Xenotransplantation., PMID:35401527
Genome-wide CRISPR/Cas9 screen identifies host factors important for porcine reproductive and respiratory syndrome virus replication., PMID:35318087
The Prognostic Significance of Proteasome 26S Subunit, Non-ATPase (PSMD) Genes for Bladder Urothelial Carcinoma Patients., PMID:34992336
Prognostic and immune infiltration signatures of proteasome 26S subunit, non-ATPase (PSMD) family genes in breast cancer patients., PMID:34839279
Development and Verification of the Amino Metabolism-Related and Immune-Associated Prognosis Signature in Gliomas., PMID:34804978
Effectiveness of bortezomib and temozolomide for eradication of recurrent human glioblastoma cells, resistant to radiation., PMID:34689859
26S Proteasome Non-ATPase Regulatory Subunits 1 (PSMD1) and 3 (PSMD3) as Putative Targets for Cancer Prognosis and Therapy., PMID:34572038
Upregulated monocyte expression of PLIN2 is associated with early arterial injury in children with overweight/obesity., PMID:34044206
Proteasome 26S subunit, non-ATPases 1 (PSMD1) and 3 (PSMD3), play an oncogenic role in chronic myeloid leukemia by stabilizing nuclear factor-kappa B., PMID:33712704
NFE2L1 and NFE2L3 Complementarily Maintain Basal Proteasome Activity in Cancer Cells through CPEB3-Mediated Translational Repression., PMID:32366381
Identification of key candidate genes involved in melanoma metastasis., PMID:31173190
Proteasome 26S Subunit, non-ATPase 3 (PSMD3) Regulates Breast Cancer by Stabilizing HER2 from Degradation., PMID:31013812
Upregulation of Proteolytic Pathways and Altered Protein Biosynthesis Underlie Retinal Pathology in a Mouse Model of Alzheimer's Disease., PMID:30707393
Identifying heterogeneous subtypes of gastric cancer and subtype‑specific subpaths of microRNA‑target pathways., PMID:29286091
Identification of key genes and construction of microRNA-mRNA regulatory networks in bladder smooth muscle cell response to mechanical stimuli using microarray expression profiles and bioinformatics analysis., PMID:29143172
2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio., PMID:29066854
Altered nucleocytoplasmic proteome and transcriptome distributions in an in vitro model of amyotrophic lateral sclerosis., PMID:28453527
Mutations in proteasome-related genes are associated with thyroid hemiagenesis., PMID:28390009
Interactome Analysis Reveals a Novel Role for RAD6 in the Regulation of Proteasome Activity and Localization in Response to DNA Damage., PMID:28031328
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome., PMID:27545680
Systematic protein-protein interaction and pathway analyses in the idiopathic inflammatory myopathies., PMID:27388770
Polymorphisms and haplotypes of the chromosome locus 17q12-17q21.1 contribute to adult asthma susceptibility in Slovenian patients., PMID:27163155
Interaction between Erythrocyte Phospholipid Fatty Acids Composition and Variants of Inflammation-Related Genes on Type 2 Diabetes., PMID:25969153
Genome-wide association study identifies a PSMD3 variant associated with neutropenia in interferon-based therapy for chronic hepatitis C., PMID:25515861
Network signatures of survival in glioblastoma multiforme., PMID:24068912
The HER2 amplicon includes several genes required for the growth and survival of HER2 positive breast cancer cells., PMID:23253899
Genetic associations with C-reactive protein level and white blood cell count in the KARE study., PMID:22788528
Human protein arginine methyltransferase 7 (PRMT7) is a type III enzyme forming ω-NG-monomethylated arginine residues., PMID:22241471
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network., PMID:22037903
Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT)., PMID:21738479
Asthma-associated polymorphisms in 17q21 influence cord blood ORMDL3 and GSDMA gene expression and IL-17 secretion., PMID:21546069
Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count., PMID:20172861
Identification of key regions and genes important in the pathogenesis of sezary syndrome by combining genomic and expression microarrays., PMID:19843862
Proteasome activator enhances survival of Huntington's disease neuronal model cells., PMID:17327906
For research use only. Not for human or drug use.
