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Human HSPD1 Knockdown Cell Line (Wb-Validated) #C61476

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RT-qPCR analysis. HeLa cells were infected with HSPD1-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. HSPD1 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 HSPD1 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:
    HSPD1
  • 货号:
    C61476
  • 应用:
  • 物种反应性:
规格:
1 Kit
价格:
询价
Information
Product Name Human HSPD1 Knockdown Cell Line (Wb-Validated)
Aliases HSPD1; Heat Shock Protein Family D (Hsp60) Member 1; HSP60; GroEL; 60 KDa Heat Shock Protein, Mitochondrial; Heat Shock 60kDa Protein 1 (Chaperonin);Heat Shock Protein Family D Member 1; Mitochondrial Matrix Protein P1; P60 Lymphocyte Protein; 60 KDa Chaperonin; Chaperonin 60; HuCHA60; HSP-60; CPN60; SPG13; Spastic Paraplegia 13 (Autosomal Dominant); Epididymis Secretory Sperm Binding Protein; Heat Shock 60kD Protein 1 (Chaperonin); Short Heat Shock Protein 60 Hsp60s1; Heat Shock Protein 65; Heat Shock Protein 60; EC 5.6.1.7; HSP65; Hsp60; HLD4
Background

Gene Name: HSPD1

NCBI Gene Entry: 3329

Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human HSPD1 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 HSPD1-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. HSPD1 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 HSPD1 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)
RT-qPCR analysis. HeLa cells were infected with HSPD1-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. HSPD1 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 HSPD1 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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