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Human HSPB8 Knockdown Cell Line (Wb-Validated) #C61129

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RT-qPCR analysis. 293T cells were infected with HSPB8-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. HSPB8 protein expression in wild-type (WT) and shRNA knockdown (KD) 293T cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against HSPB8 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:
    HSPB8
  • 货号:
    C61129
  • 应用:
  • 物种反应性:
规格:
1 Kit
价格:
询价
Information
Product Name Human HSPB8 Knockdown Cell Line (Wb-Validated)
Aliases HSPB8; Heat Shock Protein Family B (Small) Member 8; E2IG1; HSP22; CMT2L; H11; Small Stress Protein-Like Protein HSP22; Heat Shock 27kDa Protein 8; Heat Shock 22kDa Protein 8; Heat Shock Protein Beta-8; E2-Induced Gene 1 Protein; Alpha-Crystallin C Chain; Protein Kinase H11; HSPB8-N1; HSPB8-N2; DHMN2; HMN2A; CRYAC; HspB8; HMN2
Background

Gene Name: HSPB8

NCBI Gene Entry: 26353

Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human HSPB8 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. 293T cells were infected with HSPB8-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. HSPB8 protein expression in wild-type (WT) and shRNA knockdown (KD) 293T cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against HSPB8 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. 293T cells were infected with HSPB8-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. HSPB8 protein expression in wild-type (WT) and shRNA knockdown (KD) 293T cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against HSPB8 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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