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Human RUNX1 Knockdown Cell Line (Wb-Validated) #C61851

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RT-qPCR analysis. HeLa cells were infected with RUNX1-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. RUNX1 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 RUNX1 and Hsp90 α, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
  • 基因名：
    RUNX1
  • 货号：
    C61851
  • 应用：
  • 物种反应性：
规格：
1 Kit
价格：
询价

Information

Picture

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Information
Product Name Human RUNX1 Knockdown Cell Line (Wb-Validated)
Aliases RUNX1; RUNX Family Transcription Factor 1; Runt-Related Transcription Factor 1; AMLCR1; CBFA2; AML1; Polyomavirus Enhancer-Binding Protein 2 Alpha B Subunit; SL3/AKV Core-Binding Factor Alpha B Subunit; SL3-3 Enhancer Factor 1 Alpha B Subunit; Runt Related Transcription Factor 1; Acute Myeloid Leukemia 1 Protein; Oncogene AML-1; PEBP2-Alpha B; PEA2-Alpha B; PEBP2A2; Core-Binding Factor, Runt Domain, Alpha Subunit 2; Core-Binding Factor Subunit Alpha-2; AML1-EVI-1 Fusion Protein; Acute Myeloid Leukemia 1; AML1-ETO Fusion Protein; AML1-ETO Fusion; Aml1 Oncogene; Mutant RUNX1; CBF-Alpha-2; AML1-EVI-1; PEBP2alpha; CBF2alpha; PEBP2aB; EVI-1
Background

Gene Name: RUNX1

NCBI Gene Entry: 861
Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human RUNX1 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 RUNX1-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. RUNX1 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 RUNX1 and Hsp90 α, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
Citation(0)
  • 基因名：
    RUNX1
  • 货号：
    C61851
  • 应用：
  • 物种反应性：
规格：
1 Kit
价格：
询价
RELATED PRODUCTS
RT-qPCR analysis. HeLa cells were infected with RUNX1-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. RUNX1 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 RUNX1 and Hsp90 α, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
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