Desmin (DES) Mouse Monoclonal Antibody [Clone ID: UMLBI166]
Product Specifications
Background
This gene encodes a muscle-specific class III intermediate filament. Homopolymers of this protein form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane. Mutations in this gene are associated with desmin-related myopathy, a familial cardiac and skeletal myopathy (CSM), and with distal myopathies. [provided by RefSeq, Jul 2008]
Synonyms
CSM1; CSM2; LGMD2R
Gene Name
Homo sapiens desmin (DES), transcript variant 1, mRNA.
Gene ID
1674
UniProt
P17661
Conjugation
Unconjugated
Related Pathways
Arrhythmogenic right ventricular cardiomyopathy (ARVC), Dilated cardiomyopathy, Hypertrophic cardiomyopathy (HCM)
Field of Research
Arrhythmogenic right ventricular cardiomyopathy (ARVC), Dilated cardiomyopathy, Hypertrophic cardiomyopathy (HCM)
Dilution
IHC 1:200
Form
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Buffer
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Function
Druggable Genome
Storage Conditions
Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
Symbol
DES
Overview
Carrier-free (BSA/glycerol-free) Desmin mouse monoclonal antibody, clone UMLBI166
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=1674
Uniprot URL
https://www.uniprot.org/uniprot/P17661
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