Sandwich ELISA performed on whole lysate of LNCaP cells overexpressing HA-tag Bag1 protein. ELISA plate was coated with 50uL/well of chimeric human anti-HA- Tag antibody Clone RMH02 (1ug/mL) as the capture antibody. Anti-Bag1 rabbit serum was used as the detection antibody, followed by an alkaline phosphatase conjugated anti-Rabbit IgG as the Secondary antibody.
Western blot of 293T cells transfected (+) or non- transfected (-) with a DNA construct encoding HA- Tag KRas fusion protein, using anti-HA-tag rabbit monoclonal antibody (clone RM305) at 0.1 ug/mL, followed by a HRP conjugated anti-Human IgG secondary antibody.
本公司网站所展示销售的产品仅供科研!
沪公网安备 31011202007337号