|Vector Type||Mammalian Expression Vector|
|Expression Method||Constiutive, Stable / Transient|
|Selection In Mammalian Cells||Hygromycin|
A myc tag can be used in many different assays that require recognition by an antibody. If there is no antibody against the studied protein, adding a myc-tag allows one to follow the protein with an antibody against the Myc epitope. Examples are cellular localization studies by immunofluorescence or detection by Western blotting.
The peptide sequence of the myc-tag is: N-EQKLISEEDL-C (1202 Da). It can be fused to the C-terminus and the N-terminus of a protein. It is advisable not to fuse the tag directly behind the signal peptide of a secretory protein, since it can interfere with translocation into the secretory pathway.
|人 FTLS / RSPO2 基因ORF全长cDNA克隆(表达载体), C-GFPSpark 标签||HG13084-ACG|
|人 FTLS / RSPO2 基因ORF全长cDNA克隆(表达载体), C-OFPSpark 标签||HG13084-ACR|
|人 FTLS / RSPO2 基因ORF全长cDNA克隆(表达载体), C-Flag 标签||HG13084-CF|
|人 FTLS / RSPO2 基因ORF全长cDNA克隆(表达载体), C-His 标签||HG13084-CH|
|人 FTLS / RSPO2 基因ORF全长cDNA克隆(表达载体), C-Myc 标签||HG13084-CM|
|人 FTLS / RSPO2 基因ORF全长cDNA克隆(表达载体), C-HA 标签||HG13084-CY|
|人 FTLS / RSPO2 基因ORF全长cDNA(克隆载体)||HG13084-G|
|人 FTLS / RSPO2 基因ORF全长cDNA克隆(表达载体), N-Flag 标签||HG13084-NF|
|人 FTLS / RSPO2 基因ORF全长cDNA克隆(表达载体), N-His 标签||HG13084-NH|
|人 FTLS / RSPO2 基因ORF全长cDNA克隆(表达载体), N-Myc 标签||HG13084-NM|
|人 FTLS / RSPO2 基因ORF全长cDNA克隆(表达载体), N-HA 标签||HG13084-NY|
|人 FTLS / RSPO2 基因ORF全长cDNA克隆(表达载体)||HG13084-UT|
R-spondin-2, also known as RSPO2, synergizes with Wnt to activate beta-catenin. RSPO2 is secreted proteins that regulate beta-catenin signaling. Activator of the beta-catenin signaling cascade leads to TCF-dependent gene activation. Action both in the canonical Wnt / beta- catenin-dependent pathway, possibly via a direct interaction with Wnt proteins, and in a Wnt-independent beta catenin pathway through a receptor signaling pathway that may not use frizzled / LRP receptors. Probably also acts as a ligand for frizzled and LRP receptors. The encoding gene Rspo2 was identified as a novel common integration site for the mouse mammary tumor virus in viral induced mouse mammary tumors. Rspo2 and Rspo2 / Wnt1 tumors contained many spindle cells, consistent with an epithelial-mesenchymal transformation phenotype. When Rspo2 and Rspo2 / Wnt1 tumor cells were transferred into naive mice, they exhibited greater metastatic activity than cells derived from Wnt1 tumors.