Catalog No.
YHF86901
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Gly31-Gly133
Predicted molecular weight
13.77 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
Q01453
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
GAS-3, GAS3, PMP22, Peripheral myelin protein 22, PMP-22, Growth arrest-specific protein 3
Charcot-Marie-Tooth disease type 1E: clinical natural history and molecular impact of PMP22 variants., PMID:40488457
Enterovirus 71 structural viral protein 1 promotes the expression of PMP22 through m6A modification in mouse Schwann cells., PMID:40480313
CYP2C9 Promoter Variable Number Tandem Repeat Polymorphism in a Dominican Population: Exploring Differences with Genetic Ancestry., PMID:40428362
A Spanish-Portuguese GWAS of progressive supranuclear palsy reveals a novel risk locus in NFASC., PMID:40379966
Charcot-Marie-Tooth disease type 1E: Clinical Natural History and Molecular Impact of PMP22 Variants., PMID:40343019
Ferroptosis and Charcot-Marie-Tooth Disease 1A: Emerging Evidence for a Pathogenic Association., PMID:40227266
Rapid prediction of carbapenemases in Pseudomonas aeruginosa by imipenem/relebactam and MALDI-TOF MS., PMID:40130831
Repeated clear benefits of immunotherapy in a patient with Charcot-Marie-Tooth disease carrying a rare point mutation in PMP22., PMID:40126701
Guillain-Barré syndrome in patients with Charcot-Marie-Tooth type 1A disease, probably a non-random association., PMID:40120365
A case report of a MODY6 patient coexistence with Charcot-Marie-Toothe 1A syndrome., PMID:40026692
Genetic landscape of Charcot-Marie-Tooth disease in Vietnam: A prospective multicenter study., PMID:39973457
TSLP and TSLPR Expression Levels in Peripheral Blood as Potential Biomarkers in Patients with Chronic Rhinosinusitis with Nasal Polyps., PMID:39940994
Single-Cell RNA Sequencing on Formalin-Fixed and Paraffin-Embedded (FFPE) Tissue Identified Multi-Ciliary Cells in Breast Cancer., PMID:39936988
First Case of Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation Harboring Co-inherited Variants in HERC1 and PMP22 Genes from Iran: Two Novel Variants., PMID:39891458
EMP2 promotes hepatocellular carcinoma proliferation and invasion by activating cellular autophagy., PMID:39866225
Therapeutic potential of siRNA PMP22-SQ nanoparticles for Charcot-Marie-Tooth 1A neuropathy in rodents and non-human primates., PMID:39855282
Impact of psychiatric disorders on the risk of diabetic ketoacidosis in adults with type 1 diabetes mellitus: a propensity score matching case-control study., PMID:39853629
Myelin Methods: A Mini-Review., PMID:39829055
Phosphodiesterase 4D inhibition improves the functional and molecular outcome in a mouse and human model of Charcot Marie Tooth disease 1 A., PMID:39823724
Edaravone Improves Motor Dysfunction Following Brachial Plexus Avulsion Injury in Rats., PMID:39791183
Delineating the genetic landscape of Charcot-Marie-tooth disease in Türkiye: Distinct distribution, rare phenotypes, and novel variants., PMID:39776111
Prioritization of causal genes from genome-wide association studies by Bayesian data integration across loci., PMID:39774334
Disrupting the transmembrane domain interface between PMP22 and MPZ causes peripheral neuropathy., PMID:39759075
Co-Existent Central and Peripheral Demyelination: Related or Coincidental?, PMID:39728747
Predicting Time in Range Without Hypoglycaemia Using a Risk Calculator for Intermittently Scanned CGM in Type 1 Diabetes., PMID:39718005
Small-Molecule Modulators of Lipid Raft Stability and Protein-Raft Partitioning., PMID:39713458
Electrical impedance myography detects progressive pathological alterations in the hindlimb muscle of the PMP22-C3 mice, an animal model of CMT1A., PMID:39667653
Literature review of clinical analysis of hereditary neuropathy with liability to pressure palsies., PMID:39666198
The neurological damage caused by enterovirus 71 infection is associated with hsa_circ_0069335/miR-29b/PMP22 pathway., PMID:39636111
Genetically confirmed Charcot-Marie-Tooth disease type 2A manifesting with postural tremor: a case report., PMID:39604983
Mutant prevention concentrations, in vitro resistance evolution dynamics, and mechanisms of resistance to imipenem and imipenem/relebactam in carbapenem-susceptible Klebsiella pneumoniae isolates showing ceftazidime/avibactam resistance., PMID:39545736
AMOTL1 -Associated Multiple Congenital Anomalies (Craniofaciocardiohepatic Syndrome, CFCHS): A Novel Clinical Spectrum Including Craniofacial, Heart and Liver Abnormalities., PMID:39538375
The Multifaceted Role of Epithelial Membrane Protein 2 in Cancer: from Biomarker to Therapeutic Target., PMID:39428387
Assessment of the activity and mechanisms of resistance to cefiderocol and combinations of β-lactams and the novel β-lactamase inhibitors avibactam, taniborbactam, zidebactam, nacubactam, xeruborbactam, and ANT3310 in emerging double-carbapenemase-producing Enterobacterales., PMID:39382274
Deep Intraclonal Analysis for the Development of Vaccines against Drug-Resistant Klebsiella pneumoniae Lineages., PMID:39337325
High Mechanical Conditioning by Tumor Extracellular Matrix Stiffness Is a Predictive Biomarker for Antifibrotic Therapy in HER2-Negative Breast Cancer., PMID:39283720
Ultrasonographic manifestations of Charcot-Marie-Tooth disease due to a mutation in the PMP22 gene: A case image., PMID:39282721
EMP3: A promising biomarker for tumor prognosis and targeted cancer therapy., PMID:39213053
Non-immune hydrops fetalis is associated with bi-allelic pathogenic variants in the MYB Binding Protein 1a (MYBBP1A) gene., PMID:39191491
Meta-analysis of genome-wide association studies for cancer therapy-related cardiovascular dysfunction and functional mapping highlight an intergenic region close to TP63., PMID:39117733
Cervical Cancer Evades the Host Immune System through the Inhibition of Type I Interferon and CXCL9 by LIF., PMID:39078728
Quantitative proteomics unveils known and previously unrecognized alterations in neuropathic nerves., PMID:39072727
Loss of YAP in Schwann cells improves HNPP pathophysiology., PMID:38989661
Potential analgesic effect of a novel cannabidiol nanocrystals powder for the treatment of neuropathic pain., PMID:38982797
Roles for PMP22 in Schwann cell cholesterol homeostasis in health and disease., PMID:38979632
Characterization of sciatic nerve myelin sheath during development in C57BL/6 mice., PMID:38951719
DUSP1 and SOX2 expression determine squamous cell carcinoma of the salivary gland progression., PMID:38951654
Personalized Medicine in Acromegaly: The ACROFAST Study., PMID:38943661
A recurrent missense variant in ITPR3 causes demyelinating Charcot-Marie-Tooth with variable severity., PMID:38938188
For research use only. Not for human or drug use.
