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Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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Caldesmon (CALD1) exhibits functional diversity through the expression of multiple isoforms that differ in structure, localization, and biological role. CAD Antibody / Caldesmon CALD1 Isoform-Specific Functional Protein Antibody is used to detect Caldesmon (CALD1), clearly distinguishing it from the unrelated CAD enzyme, and enabling focused investigation of isoform-specific expression patterns and their functional implications.
The two major CALD1 isoform classes, high molecular weight h-caldesmon and low molecular weight l-caldesmon, represent distinct functional states of the protein. High molecular weight isoforms are associated with contractile systems and exhibit strong binding to actin filaments within organized structures, while low molecular weight isoforms are adapted for more dynamic cytoskeletal environments in non-muscle cells.
CAD Antibody, also referred to as Caldesmon antibody or CALD1 antibody, enables analysis of these isoform-specific differences by detecting CALD1 across its structural variants. Isoform distribution often reflects cellular phenotype, with contractile cells favoring high molecular weight forms and proliferative or motile cells exhibiting increased expression of lower molecular weight variants. This isoform-specific functional diversity provides insight into cellular state and behavior.
Structural differences between isoforms influence binding interactions, regulatory capacity, and cellular localization. High molecular weight caldesmon contains extended domains that support stable association with contractile filaments, whereas low molecular weight isoforms lack certain regulatory regions and are more compatible with dynamic cytoskeletal remodeling. These distinctions define the functional diversity of CALD1 across biological systems.
Isoform-specific expression is also linked to developmental stage, differentiation status, and cellular adaptation. Changes in isoform balance can indicate transitions between contractile and non-contractile states, providing a molecular signature of functional change. This makes caldesmon isoform diversity highly relevant for studies examining cellular plasticity and phenotype regulation.
Due to its ability to capture multiple CALD1 isoforms and reflect functional diversity, CAD Antibody provides a reliable tool for detecting caldesmon expression in studies focused on protein variation, cellular differentiation, and cytoskeletal adaptation. Its association with isoform-specific functional diversity supports investigation of how structural variants contribute to distinct cellular roles.
Optimal dilution of the CAD Antibody / Caldesmon CALD1 Isoform-Specific Functional Protein Antibody should be determined by the researcher.
1. Staining of formalin-fixed tissues requires boiling tissue sections in 10mM Tris with 1mM EDTA, pH 9.0, for 10-20 min followed by cooling at RT for 20 min.
2. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.
Recombinant full-length human protein was used as the immunogen for the CAD Antibody / Caldesmon CALD1 Isoform-Specific Functional Protein Antibody.
Store the CAD antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
Caldesmon antibody, CALD1 antibody, h-Caldesmon antibody, l-Caldesmon antibody, CALD1 isoform antibody, Caldesmon variant protein antibody
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