1. Antibodies
  2. Homo sapiens
  3. TRIM37

ENCAB000AMC

Antibody against Homo sapiens TRIM37

Homo sapiens
at least one cell type or tissue
awaiting characterization
Status
released
Source (vendor)
Santa Cruz Biotech
Product ID
sc-49548
Lot ID
F2507
Characterized targets
TRIM37 (Homo sapiens)
Host
goat
Clonality
polyclonal
Isotype
IgG
Antigen description
Raised against a peptide mapping at the C-terminus of TRIM37 of human origin.

Characterizations

TRIM37 (Homo sapiens)
Method: immunoprecipitation followed by mass spectrometry
Attachment PDF Icon
not reviewed
Caption
IP followed by mass spectrometry: Briefly, HeLa 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. A gel fragment corresponding to the band indicated above in the western blot image was excised and sent to the University of Alabama at Birmingham Cancer Center Mass Spectrometry/Proteomics Shared Facility. There the sample was 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, including common contaminants. Target protein is listed as hit 9a. Results in document "ENCODE_HAIB_TRIM37_(SC-49548)_03182011_MassSpec.pdf"
Submitted by
Richard Myers
Lab
Richard Myers, HAIB
TRIM37 (Homo sapiens)
Method: immunoblot
Attachment PDF Icon
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 visualized, representing strongest signal in the lane. Figure legend: IP-western with sc-49548 in whole cell lysates (WCL) of K562 and HeLa; PM=protein marker. TRIM37 band is indicated.
Submitted by
Richard Myers
Lab
Richard Myers, HAIB