Human PEDFR/PNPLA2 antibody

Adipose triglyceride lipase, Calcium-independent phospholipase A2, Desnutrin IPLA2-zeta, Pigment epithelium-derived factor receptor, TTS2.2, Transport-secretion protein 2, TTS2, ATGL, Patatin-like phospholipase domain-containing protein 2, PNPLA2

TTS2.2, TTS2, Transport-secretion protein 2, PNPLA2, Pigment epithelium-derived factor receptor, PEDF PNPLA2, Patatin-like phospholipase domain-containing protein 2, DesnutrinIPLA2-zeta, Desnutrin IPLA2-zeta, Calcium-independent phospholipase A2, ATGL, Adipose triglyceride lipase, ATGA0122-10 µg, ATGA0122-20 µg, ATGA0122-50 µg, ATGA0122-100 µg, ATGA0122-250 µg, ATGA0122-500 µg, ATGA0122-1 mg, ATGA0122-010, ATGA0122-020, ATGA0122-050, ATGA0122-100, ATGA0122-250, ATGA0122-500, ATGA0122-01M

Fischer J, et al., (2007) Nat Genet. 39 (1) : 28-30.; ; Elena S, et al., (2006) EMBO Rep. 7 (1) : 106-113.; ; Zimmermann R, et al., (2004) Science. 306 (5700) : 1383-1386.

The antibody has been tested by ELISA, Western blot, ICC/IF and FACS analysis to assure specificity and reactivity. Since application varies, however, each investigation should be titrated by the reagent to obtain optimal results.

The A431 cell lysate (40ug) was resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human ATGL antibody (1:1000) . Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system. The mouse adipose tissue lysate (40ug) was resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human ATGL antibody (1:1000) . Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system. {ATGA0122-WB2.jpg}

Flow cytometry analysis of ATGL in Hep3B cells. The cell was stained with ATGA0122 at 2-5ug for 1x10^6cells (red) . A Goat anti mouse IgG (Alexa fluor 488) was used as the secondary antibody. Mouse monoclonal IgG was used as the isotype control (dark gray), cells without incubation with primary and secondary antibody was used as the negative control (light gray) .Flow cytometry analysis of ATGL in HeLa cells. The cell was stained with ATGA0122 at 2-5ug for 1x10^6cells (red) . A Goat anti mouse IgG (Alexa fluor 488) was used as the secondary antibody. Mouse monoclonal IgG was used as the isotype control (dark gray), cells without incubation with primary and secondary antibody was used as the negative control (light gray) .{2004010103833302.jpg}

ICC/IF analysis of ATGL in Hep3B cells. The cell was stained with ATGA0122 (1:100) . The secondary antibody (green) was used Alexa Fluor 488. DAPI was stained the cell nucleus (blue) .ICC/IF analysis of ATGL in HeLa cells. The cell was stained with ATGA0122 (1:100) . The secondary antibody (green) was used Alexa Fluor 488. DAPI was stained the cell nucleus (blue) .{2004010103622287.jpg}ICC/IF analysis of ATGL in A549 cells. The cell was stained with ATGA0122 (1:100) . The secondary antibody (green) was used Alexa Fluor 488. DAPI was stained the cell nucleus (blue) .{2004010103476044.jpg} {ATGA0122-IF3b.jpg}