1X RIPA Buffer with HALT Protease and Phosphatase Inhibitors
Quelle:
Human
Formulierung:
Liquid (sterile filtered)
Application Verdünnung:
ELISA: User Optimized, ChIP: User Optimized, IP: User Optimized, WB: User Optimized
Anwendungsbeschreibung:
Human MAPK1 (ERK2) Knockout A549 Cell Lysate has been tested by SDS-PAGE and western blot and is suitable for use in Western blot, ELISA, Immunoprecipitation and ChIP. No detection of expected band at ~44kDa is observed in MAPK1 (ERK2) knockout A549 when
Western Blot of Human MAPK1 (ERK2) Knockout A549 Cell Lysate. Lane 1: Opal Prestained MW Marker (p/n MB-210-0500). Lane 2: A549 WCL Parental (p/n W09-001-372). Lane 3: A549 MAPK1 KO Clone 4. Lane 4: A549 MAPK1 KO Clone 10. Lane 5: A549 MAPK1 KO Clone 15. Lane 6: HeLa WCL Parental (p/n W09-000-364) Load: 10µg lysate/lane. Primary Antibody [Blot A] Anti-MAPK1(ERK2) (p/n 600-401-GP1) ~44kDa, [Blot B] stripped and re-probed with Anti-Tubulin (p/n 600-401-880) ~50kDa, at 1µg/mL overnight at 2-8C. Secondary Antibody: Goat Anti-Rabbit IgG HRP (p/n 611-103-122) at 1:30,000 for 1hr at RT. Block: BlockOut Buffer (p/n MB-073) for 1hr at RT. No detection of expected band at ~44kDa is observed in MAPK1 (ERK2) knockout A549 when compared with unmodified A549 cell lysates by Western blot.
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