catalog number :
MBS9126105
products full name :
TCAP Polyclonal Antibody
products short name :
[TCAP]
products name syn :
[TCAP; CMD1N; CMH25; LGMD2G; T-cap; TELE; telet honin; titin-cap]
other names :
[Telethonin; Telethonin; telethonin; titin cap protein; 19 kDa sarcomeric protein; limb girdle muscular dystrophy 2G (autosomal recessive); titin-cap; Titin cap protein]
products gene name :
[TCAP]
other gene names :
[TCAP; TCAP; TELE; CMD1N; T-cap; LGMD2G; telethonin]
uniprot entry name :
TELT_HUMAN
purity :
Affinity Purification
storage stability :
Store at -20 degree C (regular). Avoid freeze / thaw cycles.
tested application :
Western Blot (WB)
app notes :
WB: 1:500 - 1:2000
image1 heading :
Western Blot (WB)
other info1 :
Species: Human. Immunogen: Recombinant Protein. Category: Primary Antibody. Source: Rabbit
other info2 :
Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-167 of human TCAP (NP_003664.1). Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
products categories :
Polyclonal
products description :
Sarcomere assembly is regulated by the muscle protein titin. Titin is a giant elastic protein with kinase activity that extends half the length of a sarcomere. It serves as a scaffold to which myofibrils and other muscle related proteins are attached. This gene encodes a protein found in striated and cardiac muscle that binds to the titin Z1-Z2 domains and is a substrate of titin kinase, interactions thought to be critical to sarcomere assembly. Mutations in this gene are associated with limb-girdle muscular dystrophy type 2G.
ncbi mol weight :
Observed MW: 19kDa. Calculated MW: 19kDa
ncbi pathways :
Muscle Contraction Pathway (106261); Striated Muscle Contraction Pathway (198903); Striated Muscle Contraction Pathway (106262)
ncbi summary :
Sarcomere assembly is regulated by the muscle protein titin. Titin is a giant elastic protein with kinase activity that extends half the length of a sarcomere. It serves as a scaffold to which myofibrils and other muscle related proteins are attached. This gene encodes a protein found in striated and cardiac muscle that binds to the titin Z1-Z2 domains and is a substrate of titin kinase, interactions thought to be critical to sarcomere assembly. Mutations in this gene are associated with limb-girdle muscular dystrophy type 2G. [provided by RefSeq, Jul 2008]
uniprot summary :
Telethonin: a muscle assembly regulating factor that interacts with the giant kinase titin. Sarcomere assembly is regulated by the muscle protein titin. Titin is a giant elastic protein with kinase activity that extends half the length of a sarcomere. It serves as a scaffold to which myofibrils and other muscle related proteins are attached. Telethonin is found in striated and cardiac muscle that binds to the titin Z1-Z2 domains and is a substrate of titin kinase, interactions thought to be critical to sarcomere assembly. Mutations in this gene are associated with limb-girdle muscular dystrophy type 2G. Protein type: Motility/polarity/chemotaxis. Chromosomal Location of Human Ortholog: 17q12. Cellular Component: I band; cytosol; Z disc. Molecular Function: protein binding, bridging; protein binding; structural constituent of muscle; titin binding; FATZ binding. Biological Process: adult heart development; skeletal muscle contraction; cardiac muscle hypertrophy; somitogenesis; muscle thin filament assembly; detection of mechanical stimulus; cardiac myofibril assembly; sarcomere organization; muscle filament sliding; muscle thick filament assembly; cardiac muscle fiber development; cardiac muscle morphogensis; sarcomerogenesis; protein complex assembly; otic vesicle formation; cardiac muscle contraction. Disease: Muscular Dystrophy, Limb-girdle, Type 2g; Cardiomyopathy, Dilated, 1n