Mouse Desmin Monoclonal Antibody | anti-DES antibody

Desmin

Cat. Num. AAA370062

• Gene Names: DES; CSM1; CSM2; CMD1I; FLJ12025; FLJ39719; FLJ41013; FLJ41793
• Synonyms: Desmin; Monoclonal Antibody; anti-DES antibody

• Host: Mouse
• Clonality: Monoclonal
• Isotype: IgG1/K
• Clone Number: D33

• Preparation and Storage: Store at 2 to 8 degree C in the dark.

Immunohistochemistry

(IHC of Desmin on an FFPE Skeletal Muscle Tissue)

NCBI and Uniprot Product Information

• NCBI GI #: 55749932
• NCBI GeneID: 1674
• NCBI Accession #: NP_001918.3
• NCBI GenBank Nucleotide #: NM_001927.3
• UniProt Accession #: P17661; Q15787; Q8IZR1; Q8IZR6; Q8NES2; Q8NEU6; Q8TAC4; Q8TCX2; Q8TD99; Q9UHN5; Q9UJ80; Q2PUK1; Q45VM6; Q45VM7; Q45VM8; Q53SB5; Q549R7; Q549R8; Q549R9; Q5RLN0
• Molecular Weight: 53405 Da
• NCBI Official Full Name: desmin
• NCBI Official Synonym Full Names: desmin
• NCBI Official Symbol: DES
• NCBI Official Synonym Symbols: CSM1; CSM2; CMD1I; FLJ12025; FLJ39719; FLJ41013; FLJ41793
• NCBI Protein Information: desmin; OTTHUMP00000064865; intermediate filament protein
• UniProt Protein Name: Desmin
• Protein Family: Desmin
• UniProt Gene Name: DES
• UniProt Entry Name: DESM_HUMAN

NCBI Description

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]

Uniprot Description

Function: Desmin are class-III intermediate filaments found in muscle cells. In adult striated muscle they form a fibrous network connecting myofibrils to each other and to the plasma membrane from the periphery of the Z-line structures.

Subunit structure: Homopolymer. Interacts with DST

By similarity. Interacts with MTM1. Ref.10

Subcellular location: Cytoplasm.

Involvement in disease: Defects in DES are the cause of myopathy myofibrillar desmin-related (MFM-DES) [

MIM:601419]; also known as desmin-related myopathy (DRM). A neuromuscular disorder characterized by skeletal muscle weakness associated with cardiac conduction blocks, arrhythmias, restrictive heart failure, and by myofibrillar destruction with intracytoplasmic accumulation of desmin-reactive deposits in cardiac and skeletal muscle cells. Ref.4 Ref.6 Ref.7 Ref.9 Ref.13 Ref.14 Ref.15 Ref.16 Ref.17 Ref.18 Ref.19 Ref.20 Ref.22Defects in DES are the cause of cardiomyopathy dilated type 1I (CMD1I) [

MIM:604765]. Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. Ref.5Defects in DES are the cause of neurogenic scapuloperoneal syndrome Kaeser type (Kaeser syndrome) [

MIM:181400]. Kaeser syndrome is an autosomal dominant disorder with a peculiar scapuloperoneal distribution of weakness and atrophy. A large clinical variability is observed ranging from scapuloperoneal, limb grindle and distal phenotypes with variable cardiac or respiratory involvement. Facial weakness, dysphagia and gynaecomastia are frequent additional symptoms. Affected men seemingly bear a higher risk of sudden, cardiac death as compared to affected women. Histological and immunohistochemical examination of muscle biopsy specimens reveal a wide spectrum of findings ranging from near normal or unspecific pathology to typical, myofibrillar changes with accumulation of desmin.

Sequence similarities: Belongs to the intermediate filament family.