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Human RACK1 Knockdown Cell Line (Wb-Validated) #C61248

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RT-qPCR analysis. HeLa cells were infected with RACK1-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. RACK1 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 RACK1 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:
    RACK1
  • 货号:
    C61248
  • 应用:
  • 物种反应性:
规格:
1 Kit
价格:
询价
Information
Product Name Human RACK1 Knockdown Cell Line (Wb-Validated)
Aliases RACK1; Receptor For Activated C Kinase 1; GNB2L1; H12.3; Guanine Nucleotide Binding Protein (G Protein), Beta Polypeptide 2-Like 1; Guanine Nucleotide-Binding Protein Subunit Beta-Like Protein 12.3; Guanine Nucleotide-Binding Protein Subunit Beta-2-Like 1; Cell ProlifeRation-Inducing Gene 21 Protein ; Receptor Of Activated Protein C Kinase 1; Small Ribosomal Subunit Protein RACK1; Human Lung Cancer Oncogene 7 Protein ; Gnb2-Rs1; HLC-7; Protein Homologous To Chicken B Complex Protein, Guanine Nucleotide Binding; Guanine Nucleotide Binding Protein Beta Polypeptide 2-Like 1; Receptor Of Activated Protein Kinase C 1; Receptor For Activated C Kinase; ProlifeRation-Inducing Gene 21; Lung Cancer Oncogene 7; PIG21(多GNB2-RS1)
Background

Gene Name: RACK1

NCBI Gene Entry: 10399

Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human RACK1 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 RACK1-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. RACK1 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 RACK1 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 RACK1-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. RACK1 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 RACK1 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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