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Human USP39 Knockdown Cell Line (Wb-Validated) #C62621

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RT-qPCR analysis. HeLa cells were infected with USP39-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. USP39 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 USP39 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:
    USP39
  • 货号:
    C62621
  • 应用:
  • 物种反应性:
规格:
1 Kit
价格:
询价
Information
Product Name Human USP39 Knockdown Cell Line (Wb-Validated)
Aliases USP39; Ubiquitin Specific Peptidase 39; SNRNP65; CGI-21; SAD1; Small Nuclear Ribonucleoprotein 65kDa (U4/U6.U5); U4/U6.U5 Tri-SnRNP-Associated 65 KDa Protein; Ubiquitin Carboxyl-Terminal Hydrolase 39; Ubiquitin Specific Protease 39; SAD1 Homolog; SnRNP Assembly Defective 1 Homolog (S. Cerevisiae); Inactive Ubiquitin-Specific Peptidase 39; U4/U6.U5 Tri-SnRNP-Associated Protein 2; SnRNP Assembly Defective 1 Homolog; EC 3.4.19.12 ;HSPC332; 65K
Background

Gene Name: USP39

NCBI Gene Entry: 10713

Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human USP39 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 USP39-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. USP39 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 USP39 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 USP39-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. USP39 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 USP39 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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