ENCAB262WBH

Antibody against Homo sapiens HMBOX1

Homo sapiens
K562
characterized to standards
Homo sapiens
HepG2
not characterized to standards
Status
released
Source (vendor)
GeneTex
Product ID
GTX104189
Lot ID
40121
Characterized targets
HMBOX1 (Homo sapiens)
Host
rabbit
Clonality
polyclonal
Purification
affinity
Isotype
IgG
Antigen description
Recomb fragment corresp to region within amino acids 142 and 407 of HMBOX1 (Uniprot ID#Q6NT76)
External resources

Characterizations

HMBOX1 (Homo sapiens)
Method: immunoprecipitation followed by mass spectrometry
Attachment from submitter
compliant
Caption
K562 whole cell lysate was immunoprecipitated using the primary antibody (GeneTex; GTX104189). The IP fraction was loaded on a 12% Bio-Rad TGX gel and separated with the Bio-Rad Tetra Cell system. A gel fragment (rectangle outline) corresponding to the band indicated on the Coomassie Blue stained gel image was excised and sent to the University of Alabama at Birmingham Cancer Center Mass Spectrometry/Proteomics Shared Facility. Analysis of gel fragment 1 from K562: The sample was analyzed on a LTQ XL Linear Ion Trap Mass Spectrometer by LC-ESI-MS/MS. Peptides were identified using SEQUEST tandem mass spectral analysis with probability based matching at p < 0.05. SEQUEST results were reported with ProteinProphet protXML Viewer (TPP v4.4 JETSTREAM) and filtered for a minimum probability of 0.9. All protein hits that met these criteria were reported, including common contaminants. Fold enrichment for each protein reported was determined using a custom script based on the FC-B score calculation from the reference Mellacheruvu et al., 2013. The CRAPome: a contaminant repository for affinity purification mass spectrometry data. Nat. Methods. 10(8):730-736. Doi:10.1038/nmeth.2557. The target protein, HMBOX1, was identified as the 1st ranked enriched protein and the 1st ranked transcription factor based on IP-Mass Spectrometry.
Submitted by
Mark Mackiewicz
Lab
Richard Myers, HAIB
Download
HMBOX1 (Homo sapiens)
K562
Method: immunoprecipitation
Attachment from submitter
not reviewed
Reviewer comment
IP gel for mass spectrometry analysis
Submitted by
Mark Mackiewicz
Lab
Richard Myers, HAIB
HMBOX1 (Homo sapiens)
K562HepG2
Method: immunoprecipitation
Attachment from submitter
compliant
Caption
Whole cell lysates of K562 and HepG2 were immunoprecipitated using the primary antibody (GeneTex; GTX104189). The IP fraction was separated on a 12% acrylamide gel with the Bio-Rad PROTEAN II xi system. After separation, the samples were transferred to a nitrocellulose membrane with an Invitrogen iBlot system. The membrane was probed with the primary antibody (same as that used for IP) and a secondary HRP-conjugated antibody. The resulting bands were visualized with SuperSignal West Femto Solution (Thermo Scientific). Protein Marker (PM) is labeled in kDa. One band was detected at ~60 kDa. Expected size ~47-49 kDa.
Submitted by
Mark Mackiewicz
Lab
Richard Myers, HAIB