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Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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Caldesmon (CALD1) functions as a lineage-associated marker that reflects smooth muscle differentiation and cellular origin in tumor biology. CAD Antibody / Caldesmon CALD1 Tumor Differentiation Marker Antibody is used to detect Caldesmon (CALD1), clearly distinguishing it from the unrelated CAD enzyme, and enabling focused investigation of tumor differentiation and lineage identity.
In tumor systems, CALD1 expression is strongly associated with cells that retain smooth muscle characteristics, making it a valuable indicator of lineage fidelity. Tumors derived from or exhibiting smooth muscle differentiation frequently maintain caldesmon expression, whereas epithelial tumors and poorly differentiated malignancies often show reduced or absent expression. This tumor differentiation marker function provides a molecular basis for distinguishing tumor types based on lineage origin.
CAD Antibody, also referred to as Caldesmon antibody or CALD1 antibody, is widely used in studies examining tumor classification and cellular origin. Caldesmon expression provides insight into whether tumor cells retain contractile and cytoskeletal features characteristic of smooth muscle lineage. This association between CALD1 expression and lineage identity is particularly valuable when evaluating tumors with overlapping morphology.
Loss or alteration of CALD1 expression is often associated with dedifferentiation and increased cellular plasticity, reflecting a shift away from stable, contractile phenotypes toward more proliferative or invasive states. This relationship highlights the role of caldesmon as a marker of differentiation status and tumor progression.
In addition to tumor cells, caldesmon is expressed in stromal components such as myofibroblasts, which contribute to tumor architecture and microenvironment remodeling. These cells exhibit contractile features and express CALD1 as part of their cytoskeletal machinery, reinforcing its role as a marker of structurally active cell populations within tumors.
Due to its strong association with lineage identity and differentiation status, CAD Antibody provides a reliable tool for detecting CALD1 expression in studies focused on tumor biology, classification, and cellular origin. Its role as a tumor differentiation marker supports investigation of how tumors retain or lose lineage-specific characteristics.
Optimal dilution of the CAD Antibody / Caldesmon CALD1 Tumor Differentiation Marker 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 (CALD1/820) and crude human uterus extract (h-CALD) were used as the immunogen for the CAD Antibody / Caldesmon CALD1 Tumor Differentiation Marker Antibody.
Store the CAD antibody cocktail at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
Caldesmon antibody, CALD1 antibody, Caldesmon tumor marker antibody, CALD1 smooth muscle tumor antibody, h-Caldesmon antibody, Caldesmon lineage marker antibody
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