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Human NAE1 Knockdown Cell Line (Wb-Validated) #C64857

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RT-qPCR analysis. HeLa cells were infected with MYH9-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. NAE1 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. Hsp90 α served as a loading control. The blots were incubated with primary antibodies against NAE1 and Hsp90 α, respectively, followed by incubating with HRP-conjugated goat anti-mouse secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
  • 基因名:
    NAE1
  • 货号:
    C64857
  • 应用:
  • 物种反应性:
规格:
1 Kit
价格:
询价
Information
Product Name Human NAE1 Knockdown Cell Line (Wb-Validated)
Aliases NAE1; NEDD8 Activating Enzyme E1 Subunit 1; APP-BP1; APPBP1; Ula-1; Amyloid Beta Precursor Protein-Binding Protein 1, 59 KDa ; Amyloid Beta Precursor Protein Binding Protein 1, 59kDa; NEDD8-Activating Enzyme E1 Regulatory Subunit; Amyloid Protein-Binding Protein 1; Proto-Oncogene Protein 1; Amyloid Beta Precursor Protein-Binding Protein 1, 59kD; NEDD8-Activating Enzyme E1 Subunit; Protooncogene Protein 1; A-116A10.1; NEDFIH; HPP1
Background

Gene Name: NAE1

NCBI Gene Entry: 8883

Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human NAE1 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 MYH9-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. NAE1 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. Hsp90 α served as a loading control. The blots were incubated with primary antibodies against NAE1 and Hsp90 α, respectively, followed by incubating with HRP-conjugated goat anti-mouse secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
Citation(0)
RT-qPCR analysis. HeLa cells were infected with MYH9-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. NAE1 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. Hsp90 α served as a loading control. The blots were incubated with primary antibodies against NAE1 and Hsp90 α, respectively, followed by incubating with HRP-conjugated goat anti-mouse secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
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