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Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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Caldesmon (CALD1) is an actin- and myosin-binding regulatory protein that plays a central role in smooth muscle contraction and cytoskeletal organization. Caldesmon Antibody for WB (clone SPM168) is designed for western blot detection of CALD1, enabling detailed analysis of its isoform-dependent migration patterns and expression across different cell types.
Caldesmon Antibody for WB (clone SPM168) supports clear interpretation of CALD1 banding behavior in western blot experiments, where multiple isoforms produce distinct molecular weight signals. Caldesmon antibody, also referred to as CALD1 antibody or h-caldesmon antibody, is particularly valuable in western blot analysis because CALD1 does not resolve as a single band. Instead, a predicted molecular weight of approximately 93 kDa is often accompanied by lower molecular weight bands at approximately 70-80 kDa in non-muscle cells and higher molecular weight bands at approximately 120-150 kDa corresponding to the smooth muscle-associated h-caldesmon isoform.
This Caldesmon Antibody for WB (clone SPM168) is uniquely positioned for isoform-resolved western blot detection, allowing researchers to distinguish between contractile smooth muscle-associated forms and lower molecular weight cytoskeletal variants. The observed migration differences reflect isoform composition and structural variation rather than simple degradation, making accurate band interpretation critical when analyzing CALD1 expression. Clone SPM168 antibody enables consistent detection of these bands, supporting reliable comparison between tissue types and experimental conditions.
At the molecular level, CALD1 produces high molecular weight and low molecular weight isoforms that serve distinct biological roles. The high molecular weight h-caldesmon isoform is enriched in differentiated smooth muscle cells and is closely associated with actomyosin regulation and contractile function. In contrast, lower molecular weight isoforms are more broadly expressed and contribute to cytoskeletal remodeling in non-muscle cells. Western blot analysis using Caldesmon Antibody for WB (clone SPM168) enables direct visualization of these isoform-specific differences, providing insight into cellular phenotype and functional state.
Due to its strong performance in western blot applications and its ability to resolve multiple CALD1 isoforms across a wide molecular weight range, Caldesmon Antibody for WB (clone SPM168) provides a reliable tool for detecting caldesmon expression in studies focused on muscle biology, cytoskeletal regulation, and cellular differentiation. Its consistent banding patterns and alignment with known CALD1 isoform biology support confident interpretation of western blot results in both smooth muscle and non-muscle systems.
Optimal dilution of the Caldesmon Antibody for WB / CALD1 Western Blot 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, 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.
Crude human uterus extract was used as the immunogen for the Caldesmon Antibody for WB / CALD1 Western Blot Antibody.
Store the Caldesmon antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
Caldesmon antibody, CALD1 antibody, Caldesmon western blot antibody, CALD1 WB antibody, h-Caldesmon antibody, Caldesmon isoform antibody
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