The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Use 1µg for 106 cells.
ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody.
Use a concentration of 1 - 2 µg/ml. Detects a band of approximately 31 kDa.
Protects against apoptosis induced by TNF or by chemical agents such as adriamycin, etoposide or staurosporine. Suppression of apoptosis is mediated by activation of MAPK8/JNK1, and possibly also of MAPK9/JNK2. This activation depends on TAB1 and NR2C2/TAK1. In vitro, inhibits caspase-3 and proteolytic activation of pro-caspase-9. Isoform 1 blocks staurosporine-induced apoptosis. Isoform 2 blocks etoposide-induced apoptosis.
Isoform 1 and isoform 2 are expressed at very low levels or not detectable in most adult tissues. Detected in adult heart, placenta, lung, lymph node, spleen and ovary, and in several carcinoma cell lines. Isoform 2 is detected in fetal kidney, heart and spleen, and at lower levels in adult brain, skeletal muscle and peripheral blood leukocytes.
Belongs to the IAP family. Contains 1 BIR repeat. Contains 1 RING-type zinc finger.
Nucleus. Cytoplasm. Nuclear, and in a filamentous pattern throughout the cytoplasm.
Baculoviral IAP repeat containing protein 7 antibody
Baculoviral IAP repeat-containing protein 7 antibody
BIRC 7 antibody
Kidney inhibitor of apoptosis protein antibody
Livin inhibitor of apotosis antibody
Melanoma inhibitor of apoptosis protein antibody
ML IAP antibody
RING finger protein 50 antibody
RNF 50 antibody
Western blot - Anti-Livin antibody [88C570] (ab11983)
Livin detection by Western blot. The detection of Livin in cell extract transfected with human Livin cDNA. A protein of 31 kDa was detected by using anti-Livin at a 2 µg/ml dilution. Livin detection by Western blot. The detection of Livin in cell extract transfected with human Livin cDNA. A protein of 31 kDa was detected by using anti-Livin at a 2 µg/ml dilution.
Overlay histogram showing HeLa cells stained with ab11983 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab11983, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.