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Human PSME1 Knockdown Cell Line (Wb-Validated) #C62582

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RT-qPCR analysis. HeLa cells were infected with PSME1-specific shRNA lentiviral particles, total RNA was extracted from wild-type and knockdown cells, RT-qPCR was performed using gene-specific primers. ∆Ct (CtKD-CtWT) was used to calculate mRNA reduction (%) between wild-type and knockdown cells using the following formula: (1-1/2∆Ct) x 100%.
Western blotting analysis. PSME1 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against PSME1 and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
  • 基因名:
    PSME1
  • 货号:
    C62582
  • 应用:
  • 物种反应性:
规格:
1 Kit
价格:
询价
Information
Product Name Human PSME1 Knockdown Cell Line (Wb-Validated)
Aliases PSME1; Proteasome Activator Subunit 1; PA28alpha; IFI5111; Proteasome (Prosome, Macropain) Activator Subunit 1 (PA28 Alpha); Activator Of Multicatalytic Protease Subunit 1; Interferon Gamma Up-Regulated I-5111 Protein; Proteasome Activator Complex Subunit 1; 11S Regulator Complex Subunit Alpha; IGUP I-5111; Epididymis Secretory Sperm Binding Protein Li 129m; Interferon-Gamma-Inducible Protein 5111; Proteasome Activator 28 Subunit Alpha; Interferon-Gamma IEF SSP 5111; 29-KD MCP Activator Subunit; HEL-S-129m; REG-Alpha; REGalpha; PA28A; PA28a
Background

Gene Name: PSME1

NCBI Gene Entry: 5720

Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human PSME1 Knockdown Cell Line (Wb-Validated)
2. Wild-type cell line
Parental Cell Line Human cell line supplied by the client
Validation Methods RT-qPCR, Western blotting (WB)
Shipping Shipped on Dry Ice.
Instructions For Use This knockdown cell line should be paired with wild-type cell line for use.
Note This product is for research use only.
Picture
  • RT-qPCR analysis. HeLa cells were infected with PSME1-specific shRNA lentiviral particles, total RNA was extracted from wild-type and knockdown cells, RT-qPCR was performed using gene-specific primers. ∆Ct (CtKD-CtWT) was used to calculate mRNA reduction (%) between wild-type and knockdown cells using the following formula: (1-1/2∆Ct) x 100%.
  • Western blotting analysis. PSME1 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against PSME1 and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
Citation(0)
RT-qPCR analysis. HeLa cells were infected with PSME1-specific shRNA lentiviral particles, total RNA was extracted from wild-type and knockdown cells, RT-qPCR was performed using gene-specific primers. ∆Ct (CtKD-CtWT) was used to calculate mRNA reduction (%) between wild-type and knockdown cells using the following formula: (1-1/2∆Ct) x 100%.
Western blotting analysis. PSME1 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against PSME1 and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
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