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Human CHUK Knockdown Cell Line (Wb-Validated) #C1374

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RT-qPCR analysis. HeLa cells were infected with CHUK-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. CHUK 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 (Cat#61374, 1:5,000) against CHUK and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000). Images were developed using FeQ™ ECL Substrate Kit (Cat#226).
  • 基因名:
    CHUK
  • 货号:
    C1374
  • 应用:
  • 物种反应性:
规格:
1 Kit
价格:
询价
Information
Product Name Human CHUK Knockdown Cell Line (Wb-Validated)
Aliases CHUK; Component Of Inhibitor Of Nuclear Factor Kappa B Kinase Complex; IKK-Alpha; NFKBIKA; IKK1; IKKA; Inhibitor Of Nuclear Factor Kappa-B Kinase Subunit Alpha; Conserved Helix-Loop-Helix Ubiquitous Kinase; IkBKA; TCF16; Transcription Factor 16; I-Kappa-B Kinase 1; EC 2.7.11.10; IKK-1; Nuclear Factor NF-Kappa-B Inhibitor Kinase Alpha; Nuclear Factor NFkappaB Inhibitor Kinase Alpha; IkB Kinase Alpha Subunit; I-Kappa-B Kinase-Alpha; I-Kappa-B Kinase Alpha; I-Kappa-B Kinase; IkappaB Kinase; IKK-A Kinase; EC 2.7.11; TCF-16; IKBKA; IKK-A; BPS2
Background

Gene Name: CHUK

NCBI Gene Entry: 1147

Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human CHUK 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 CHUK-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. CHUK 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 (Cat#61374, 1:5,000) against CHUK and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000). Images were developed using FeQ™ ECL Substrate Kit (Cat#226).
Citation(0)
RT-qPCR analysis. HeLa cells were infected with CHUK-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. CHUK 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 (Cat#61374, 1:5,000) against CHUK and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000). Images were developed using FeQ™ ECL Substrate Kit (Cat#226).
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