The STAC3 Monoclonal Antibody (PACO38754) is a powerful tool for researchers studying STAC3, a key protein involved in skeletal muscle function and calcium channel regulation. This antibody is produced through a highly specific monoclonal process, ensuring reliable and reproducible results in various experimental applications. STAC3 is known to play a crucial role in the regulation of excitation-contraction coupling in skeletal muscle, making it a promising target for studies on muscle physiology and muscle-related disorders.
The STAC3 Monoclonal Antibody binds specifically to the STAC3 protein, enabling precise detection and analysis in different cell and tissue types.Researchers in the fields of muscle biology, neuroscience, and pharmacology can benefit from the use of the STAC3 Monoclonal Antibody in their investigations. By understanding the function and regulation of STAC3, new insights may be gained into muscle contraction mechanisms, calcium signaling pathways, and potential therapeutic interventions for muscle disorders.
Antibody Name:
STAC3 Antibody (PACO38754)
Antibody SKU:
PACO38754
Size:
50ug
Host Species:
Rabbit
Tested Applications:
ELISA, WB
Recommended Dilutions:
ELISA:1:2000-1:10000, WB:1:500-1:2000
Species Reactivity:
Human, Rat
Immunogen:
Recombinant Human SH3 and cysteine-rich domain-containing protein 3 protein (1-253AA)
Western blot. All lanes: STAC3 antibody at 12µg/ml + Rat lung tissue. Secondary. Goat polyclonal to rabbit IgG at 1/10000 dilution. Predicted band size: 42, 38, 21 kDa. Observed band size: 42 kDa.
Background:
In skeletal muscles contraction, may play a role in neuromuscular synaptic transmission.
Synonyms:
SH3 and cysteine-rich domain-containing protein 3, STAC3
UniProt Protein Function:
UniProt Protein Details:
NCBI Summary:
The protein encoded by this gene is a component of the excitation-contraction coupling machinery of muscles. This protein is a member of the Stac gene family and contains an N-terminal cysteine-rich domain and two SH3 domains. Mutations in this gene are a cause of Native American myopathy. [provided by RefSeq, Nov 2013]
