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SCARA3 encodes a macrophage scavenger receptor-like protein. Additionally we are shipping SCARA3 Antibodies (28) and SCARA3 Proteins (5) and many more products for this protein.
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The interaction between CSR1 and SF3A3 (show SF3A3 ELISA Kits) led to migration of SF3A3 (show SF3A3 ELISA Kits) from nucleus to cytoplasm. The cytoplasmic redistribution of SF3A3 (show SF3A3 ELISA Kits) significantly reduced the splicing efficiency of epidermal growth factor receptor (show EGFR ELISA Kits) and platelet-derived growth factor receptor (show PDGFRL ELISA Kits).
Suppression of CSR1 expression is a novel mechanism critical for the oncogenic activity of miR (show MLXIP ELISA Kits)-650.
Findings regarding the interaction of NADPH-P450 reductase (NPR (show POR ELISA Kits)) with cellular stress response (CSR) indicated function of NPR (show NPTXR ELISA Kits) in hypoxic response.
Data indicate that the clinical samples showed an inverse correlation between SCARA3 gene expression, myeloma progression, and favorable clinical prognosis.
The binding of CSR1 with XIAP (show XIAP ELISA Kits) enhanced caspase-9 (show CASP9 ELISA Kits) and caspase-3 (show CASP3 ELISA Kits) protease activities.
The consistently high SCARA3 levels in both primary carcinomas and metastatic cells in effusions, and its up-regulation along disease progression from diagnosis to recurrence, suggest a role in ovarian cancer biology.
Results demonstrate the involvement of SCARA3 and SCARA5 (show SCARA5 ELISA Kits) in the uptake of PF14-oligonucleotide nanocomplexes.
Down-regulation of CSR1 protein expression by promoter methylation is associated with tumor growth and metastasis of prostate cancer
CSR1 appears to induce cell death through a novel mechanism by hijacking a critical RNA processing enzyme CPSF3 (show CPSF3 ELISA Kits).
This gene encodes a macrophage scavenger receptor-like protein. This protein has been shown to deplete reactive oxygen species, and thus play an important role in protecting cells from oxidative stress. The expression of this gene is induced by oxidative stress. Alternatively spliced transcript variants encoding distinct isoforms have been described.
cellular stress response gene protein
, cellular stress response protein
, macrophage scavenger receptor-like 1
, scavenger receptor class A member 3
, scavenger receptor class A, member 3
, scavenger receptor class A member 3-like