Catalog No.
YHK94201
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Met1-Lys180
Predicted molecular weight
22.46 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
Q5T8D3-2
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
ACBD5, KIAA1996, Acyl-CoA-binding domain-containing protein 5
ACOT12, a novel factor in the pathogenesis of kidney fibrosis, modulates ACBD5., PMID:39939783
A Novel Peroxisome-Related Gene Signature Predicts Breast Cancer Prognosis and Correlates with T Cell Suppression., PMID:39678026
Quantitative proteomics combined independent PRM analysis reveals the mitochondrial and synaptic mechanism underlying norisoboldine's antidepressant effects., PMID:39358323
New insights into the functions of ACBD4/5-like proteins using a combined phylogenetic and experimental approach across model organisms., PMID:39271061
Multifocal Papillary Thyroid Carcinomas With Discordant Molecular Drivers: Emphasizing the Morphology and Collision Tumors., PMID:38818543
Ganoderic acid A ameliorates depressive-like behaviors in CSDS mice: Insights from proteomic profiling and molecular mechanisms., PMID:38723681
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders., PMID:37951597
Hepatitis C virus alters the morphology and function of peroxisomes., PMID:37808318
ACBD5-related retinal dystrophy with leukodystrophy due to novel mutations in ACBD5 and with additional features including ovarian insufficiency., PMID:37789430
Differential roles for ACBD4 and ACBD5 in peroxisome-ER interactions and lipid metabolism., PMID:37414147
Metabolome-Based Genome-Wide Association Study of Duck Meat Leads to Novel Genetic and Biochemical Insights., PMID:37013465
Assessing Peroxisomal Protein Interaction by Immunoprecipitation., PMID:36952197
Restructured membrane contacts rewire organelles for human cytomegalovirus infection., PMID:35953480
Fission Impossible (?)-New Insights into Disorders of Peroxisome Dynamics., PMID:35741050
Multiple Ways to Keep FFAT Under Control!, PMID:35611050
Regulating peroxisome-ER contacts via the ACBD5-VAPB tether by FFAT motif phosphorylation and GSK3β., PMID:35019937
Newly defined peroxisomal disease with novel ACBD5 mutation., PMID:34668366
First reported adult patient with retinal dystrophy and leukodystrophy caused by a novel ACBD5 variant: A case report and review of literature., PMID:33427402
Cerebellar and hepatic alterations in ACBD5-deficient mice are associated with unexpected, distinct alterations in cellular lipid homeostasis., PMID:33244184
Fluorescent tools to analyse peroxisome-ER interactions in mammalian cells., PMID:31198905
Organelle interplay-peroxisome interactions in health and disease., PMID:30864148
Intracellular redistribution of neuronal peroxisomes in response to ACBD5 expression., PMID:30589881
The peroxisome: an update on mysteries 2.0., PMID:30219925
Peroxisome Motility Measurement and Quantification Assay., PMID:28936467
Functional characterisation of peroxisomal β-oxidation disorders in fibroblasts using lipidomics., PMID:28849344
Predicting the targeting of tail-anchored proteins to subcellular compartments in mammalian cells., PMID:28325759
Incredibly close-A newly identified peroxisome-ER contact site in humans., PMID:28108527
VAPs and ACBD5 tether peroxisomes to the ER for peroxisome maintenance and lipid homeostasis., PMID:28108526
ACBD5 and VAPB mediate membrane associations between peroxisomes and the ER., PMID:28108524
Deficiency of a Retinal Dystrophy Protein, Acyl-CoA Binding Domain-containing 5 (ACBD5), Impairs Peroxisomal β-Oxidation of Very-long-chain Fatty Acids., PMID:27899449
ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism., PMID:27799409
Relationships between Circulating Urea Concentrations and Endometrial Function in Postpartum Dairy Cows., PMID:26479384
Using SILAC proteomics to investigate the effect of the mycotoxin, alternariol, in the human H295R steroidogenesis model., PMID:25416481
A novel RET rearrangement (ACBD5/RET) by pericentric inversion, inv(10)(p12.1;q11.2), in papillary thyroid cancer from an atomic bomb survivor exposed to high-dose radiation., PMID:25175022
Atg37 regulates the assembly of the pexophagic receptor protein complex., PMID:24905344
Peroxisomal Atg37 binds Atg30 or palmitoyl-CoA to regulate phagophore formation during pexophagy., PMID:24535825
Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2., PMID:21211618
A mutation in the acyl-coenzyme A binding domain-containing protein 5 gene (ACBD5 ) identified in autosomal dominant thrombocytopenia., PMID:20626622
Improved method for analysis of RNA present in long-term preserved thyroid cancer tissue of atomic bomb survivors., PMID:19785523
For research use only. Not for human or drug use.
