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DTNA (Dystrobrevin alpha) mouse monoclonal antibody, clone OTI1B11 (formerly 1B11)
Cat Number: GAM613294
DTNA (Dystrobrevin alpha) mouse monoclonal antibody, clone OTI1B11 (formerly 1B11)
Applications:
FCIFWB
Species Reactivity:
HumanMouseRat
$ 169
/ 50ul
In Stock
50ul100ul
Description
Recommended Dilution
Product Features
Applications
FCIFWB
Species Reactivity
HumanMouseRat
Uniprot
Q9Y4J8
Isotype
IgG2b
Background
The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq]
Calculated molecular weight
58.7 kDa
Purification method
Affinity Purification
Clonality
Monoclonal
Host species
Mouse
Immunogen
Full length human recombinant protein of human DTNA (NP_116761) produced in HEK293T cell.
Clone name
OTI1B11
Alias
DTNA
Cat Number: GAM613294
DTNA (Dystrobrevin alpha) mouse monoclonal antibody, clone OTI1B11 (formerly 1B11)
Applications:
FCIFWB
Species Reactivity:
HumanMouseRat
$ 169
/ 50ul
In Stock
50ul100ul
Description
Recommended Dilution
Product Features
Applications
FCIFWB
Species Reactivity
HumanMouseRat
Uniprot
Q9Y4J8
Isotype
IgG2b
Background
The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq]
Calculated molecular weight
58.7 kDa
Purification method
Affinity Purification
Clonality
Monoclonal
Host species
Mouse
Immunogen
Full length human recombinant protein of human DTNA (NP_116761) produced in HEK293T cell.
Clone name
OTI1B11
Alias
DTNA
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