Product Name
PSMC5 Recombinant Rabbit Monoclonal Antibody [PSH0-22] - BSA and Azide free
Antibody Type
Recombinant Rabbit monoclonal Antibody
Immunogen
Recombinant protein within Human PSMC5 aa 207-406 / 406.
Target Molecular Weight
Predicted band size: 46 kDa
Positive Control
A431 cell lysate, MCF-7 cell lysate, Hela cell lysate, HepG2 cell lysate, 293T cell lysate, NIH/3T3 cell lysate, PC-12 cell lysate, mouse testis tissue lysate, mouse heart tissue lysate, rat testis tissue lysate, rat brain tissue lysate, human lung carcinoma tissue, mouse brain tissue, rat brain tissue.
Storage Instructions
Store at 2-8℃. Avoid freeze.
Purification Method
Protein A affinity purified.
Function
The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes one of the ATPase subunits, a member of the triple-A family of ATPases which have a chaperone-like activity. In addition to participation in proteasome functions, this subunit may participate in transcriptional regulation since it has been shown to interact with the thyroid hormone receptor and retinoid X receptor-alpha. Two transcript variants encoding different isoforms have been found for this gene.
Background References
1. He Z et al. PSMC5 Promotes Proliferation and Metastasis of Colorectal Cancer by Activating Epithelial-Mesenchymal Transition Signaling and Modulating Immune Infiltrating Cells. Front Cell Dev Biol. 2021 Jul
2. Zavodszky E et al. Identification of a quality-control factor that monitors failures during proteasome assembly. Science. 2021 Aug
Synonyms
26S protease regulatory subunit 8 antibody
26S proteasome AAA-ATPase subunit RPT6 antibody
Cim3 antibody
MSUG1 protein antibody
p45 antibody
p45/SUG antibody
Proteasome 26S ATPase subunit 5 antibody
Proteasome 26S subunit ATPase 5 antibody
Proteasome prosome macropain 26S subunit ATPase 5 antibody
Proteasome subunit p45 antibody
Expand
26S protease regulatory subunit 8 antibody
26S proteasome AAA-ATPase subunit RPT6 antibody
Cim3 antibody
MSUG1 protein antibody
p45 antibody
p45/SUG antibody
Proteasome 26S ATPase subunit 5 antibody
Proteasome 26S subunit ATPase 5 antibody
Proteasome prosome macropain 26S subunit ATPase 5 antibody
Proteasome subunit p45 antibody
PRS8_HUMAN antibody
PSMC5 antibody
Rpt6 antibody
S8 antibody
SUG1 antibody
Tat binding protein homolog 10 antibody
TBP10 antibody
Thyroid hormone receptor interacting protein 1 antibody
Thyroid hormone receptor-interacting protein 1 antibody
Thyroid receptor interactor 1 antibody
TRIP1 antibody
TRIP1(SUG1) antibody
Collapse
-
This data was developed using HA721301, the same antibody clone in a different buffer formulation.
Western blot analysis of PSMC5 on different lysates with Rabbit anti-PSMC5 antibody (HA721301) at 1/1,000 dilution.
Lane 1: A431 cell lysate (20 µg/Lane)
Lane 2: MCF-7 cell lysate (20 µg/Lane)
Lane 3: Hela cell lysate (20 µg/Lane)
Lane 4: HepG2 cell lysate (20 µg/Lane)
Lane 5: 293T cell lysate (20 µg/Lane)
Lane 6: NIH/3T3 cell lysate (20 µg/Lane)
Lane 7: PC-12 cell lysate (20 µg/Lane)
Lane 8: Mouse testis tissue lysate (40 µg/Lane)
Lane 9: Mouse heart tissue lysate (40 µg/Lane)
Lane 10: Rat testis tissue lysate (40 µg/Lane)
Lane 11: Rat brain tissue lysate (40 µg/Lane)
Predicted band size: 46 kDa
Observed band size: 46 kDa
Exposure time: 30 seconds;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721301) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature.
-
This data was developed using HA721301, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue with Rabbit anti-PSMC5 antibody (HA721301) at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721301) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
-
This data was developed using HA721301, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-PSMC5 antibody (HA721301) at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721301) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
-
This data was developed using HA721301, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-PSMC5 antibody (HA721301) at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721301) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"