Product Name
PSMD13 Recombinant Rabbit Monoclonal Antibody [PSH0-52] - BSA and Azide free
Antibody Type
Recombinant Rabbit monoclonal Antibody
Immunogen
Recombinant protein within human PSMD13 aa 1-150/376.
Target Molecular Weight
Predicted band size: 43 kDa
Positive Control
HeLa cell lysate, Jurkat cell lysate, HepG2 cell lysate, SiHa cell lysate, HEK-293 cell lysate, SH-SY5Y cell lysate, NIH/3T3 cell lysate, PC-12 cell lysate, mouse testis tissue lysate, rat testis tissue lysate, human brain tissue, rat brain tissue, HeLa.
Storage Instructions
Store at 2-8℃. Avoid freeze.
Purification Method
Protein A affinity purified.
Function
26S proteasome non-ATPase regulatory subunit 13 is an enzyme that in humans is encoded by the PSMD13 gene. 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 a non-ATPase subunit of the 19S regulator. Two transcripts encoding different isoforms have been described.
Background References
1. He S et al. Alternative splicing of PSMD13 mediated by genetic variants is significantly associated with endometrial cancer risk. J Gynecol Oncol. 2023 Jan
2. Martínez-Fernández C et al. BAP1 Malignant Pleural Mesothelioma Mutations in Caenorhabditis elegans Reveal Synthetic Lethality between ubh-4/BAP1 and the Proteasome Subunit rpn-9/PSMD13. Cells. 2023 Mar
Subcellular Location
Proteasome, cytosol, extracellular region, nucleoplasm, nucleus.
Synonyms
26S proteasome non ATPase regulatory subunit 13 antibody
26S proteasome non-ATPase regulatory subunit 13 antibody
26S proteasome regulatory subunit p40.5 antibody
26S proteasome regulatory subunit RPN9 antibody
26S proteasome regulatory subunit S11 antibody
26S proteasome subunit p40.5 antibody
HSPC027 antibody
P40.5 antibody
Proteasome (prosome, macropain) 26S subunit, non ATPase, 13 antibody
Proteasome 26S subunit, non-ATPase 13 antibody
Expand
26S proteasome non ATPase regulatory subunit 13 antibody
26S proteasome non-ATPase regulatory subunit 13 antibody
26S proteasome regulatory subunit p40.5 antibody
26S proteasome regulatory subunit RPN9 antibody
26S proteasome regulatory subunit S11 antibody
26S proteasome subunit p40.5 antibody
HSPC027 antibody
P40.5 antibody
Proteasome (prosome, macropain) 26S subunit, non ATPase, 13 antibody
Proteasome 26S subunit, non-ATPase 13 antibody
PSD13_HUMAN antibody
psmD13 antibody
Rpn9 antibody
S11 antibody
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This data was developed using HA721399, the same antibody clone in a different buffer formulation.
Western blot analysis of PSMD13 on different lysates with Rabbit anti-PSMD13 antibody (HA721399) at 1/1,000 dilution.
Lane 1: HeLa cell lysate
Lane 2: Jurkat cell lysate
Lane 3: HepG2 cell lysate
Lane 4: SiHa cell lysate
Lane 5: HEK-293 cell lysate
Lane 6: SH-SY5Y cell lysate
Lane 7: NIH/3T3 cell lysate
Lane 8: PC-12 cell lysate
Lane 9: Mouse testis tissue lysate
Lane 10: Rat testis tissue lysate
Lysates/proteins at 20 µg/Lane.
Predicted band size: 43 kDa
Observed band size: 43 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 (HA721399) 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 1:100,000 dilution was used for 1 hour at room temperature.
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This data was developed using HA721399, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-PSMD13 antibody (HA721399) at 1/200 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 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 (HA721399) at 1/200 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.
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This data was developed using HA721399, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-PSMD13 antibody (HA721399) at 1/200 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 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 (HA721399) at 1/200 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.
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This data was developed using HA721399, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of HeLa cells labeling PSMD13 with Rabbit anti-PSMD13 antibody (HA721399) at 1/200 dilution.
Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-PSMD13 antibody (HA721399) at 1/200 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI.
Beta tubulin (M1305-2, red) was stained at 1/200 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"