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Human MIB1 Knockdown Cell Line (Wb-Validated) #C65263

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RT-qPCR analysis. HT-1080 cells were infected with MIB1-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.MIB1 protein expression in wild-type (WT) and shRNA knockdown (KD) HT-1080 cells was detected using Western blotting.  Hsp90 α served as a loading control. The blots were incubated with primary antibodies against MIB1 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：
    MIB1
  • 货号：
    C65263
  • 应用：
  • 物种反应性：
规格：
1 Kit
价格：
询价

Information

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Information
Product Name Human MIB1 Knockdown Cell Line (Wb-Validated)
Aliases MIB1; MIB E3 Ubiquitin Protein Ligase 1; ZZANK2; DIP-1; DAPK-Interacting Protein 1; KIAA1323; ZZZ6; MIB; Zinc Finger ZZ Type With Ankyrin Repeat Domain Protein; RING-Type E3 Ubiquitin Transferase MIB1; E3 Ubiquitin-Protein Ligase MIB1; DIP1; Mindbomb E3 Ubiquitin Protein Ligase 1; Mindbomb Homolog 1 (Drosophila); Ubiquitin Ligase Mind Bomb; Mind Bomb Homolog 1; EC 2.3.2.27; EC 6.3.2; LVNC7
Background

Gene Name: MIB1

NCBI Gene Entry: 57534
Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human MIB1 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. HT-1080 cells were infected with MIB1-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.MIB1 protein expression in wild-type (WT) and shRNA knockdown (KD) HT-1080 cells was detected using Western blotting.  Hsp90 α served as a loading control. The blots were incubated with primary antibodies against MIB1 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：
    MIB1
  • 货号：
    C65263
  • 应用：
  • 物种反应性：
规格：
1 Kit
价格：
询价
RELATED PRODUCTS
RT-qPCR analysis. HT-1080 cells were infected with MIB1-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.MIB1 protein expression in wild-type (WT) and shRNA knockdown (KD) HT-1080 cells was detected using Western blotting.  Hsp90 α served as a loading control. The blots were incubated with primary antibodies against MIB1 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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