ENCAB000AHZ
Antibody against Homo sapiens IRF4
Homo sapiens
at least one cell type or tissue
awaiting characterization
- Status
- released
- Source (vendor)
- Santa Cruz Biotech
- Product ID
- sc-6059
- Lot ID
- IO1O6
- Characterized targets
- IRF4 (Homo sapiens)
- Host
- goat
- Clonality
- polyclonal
- Isotype
- IgG
- Antigen description
- Epitope mapping at the C-terminus of IRF-4 of mouse origin.
- External resources
Characterizations
IRF4 (Homo sapiens)
not reviewed
- Caption
- Western blot protocol: Whole cell lysate was immunoprecipitated using primary antibody, and the IP fraction was loaded on a 12% acrylamide gel and separated with a Bio-Rad PROTEAN II xi system. After separation, the samples were transferred to a nitrocellulose membrane with an Invitrogen iBlot system. Blotting with primary (same as that used for IP) and secondary HRP-conjugated antibodies was performed on an Invitrogen BenchPro 4100 system. Visualization was achieved using SuperSignal West Femto solution (Thermo Scientific). Results: Band of expected size (52 kDa) visualized, representing strongest signal in the lane. IRF4 is not expressed in K562 and therefore serves as a negative control. Figure legend: IP-western with sc-6059 in whole cell lysate (WCL) of GM12878 and K562; PM=protein marker. IRF4 band is indicated. IRF4 is not expressed in K562 and therefore serves as a negative control.
- Submitted by
- Richard Myers
- Lab
- Richard Myers, HAIB
- Grant
- U54HG004576
IRF4 (Homo sapiens)
not reviewed
- Caption
- IP followed by mass spectrometry: Briefly, GM12878 whole cell lysates were immunoprecipitated using primary antibody, and the IP fraction was loaded on a 12% acrylamide gel and separated with a Bio-Rad PROTEAN II xi system. Gel was stained with Coomassie Blue in order to visualize marker bands. Gel fragments corresponding to the bands indicated above in the western blot image were excised and sent to the University of Alabama at Birmingham Cancer Center Mass Spectrometry/Proteomics Shared Facility. There the samples were run on an LTQ XL Linear Ion Trap Mass Spectrometer by LC-ESI-MS/MS. Peptides were identified using SEQUEST tandem mass spectra analysis, with probability based matching at p < 0.05. As per ENCODE data standards, all SEQUEST results are attached (ENCODE_HAIB_IRF4_sc6059_09122011_MassSpec.pdf), including common contaminants. Target protein is listed as hit 6 in ~50 kDa band.
- Submitted by
- Richard Myers
- Lab
- Richard Myers, HAIB
- Grant
- U54HG004576