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Human TAF1C Knockdown Cell Line (Wb-Validated) #C65610

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RT-qPCR analysis. HT-1080 cells were infected with TAF1C-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.TAF1C 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 TAF1C and Hsp90 α, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using NaQ™ ECL Substrate Kit.
  • 基因名:
    TAF1C
  • 货号:
    C65610
  • 应用:
  • 物种反应性:
规格:
1 Kit
价格:
询价
Information
Product Name Human TAF1C Knockdown Cell Line (Wb-Validated)
Aliases TAF1C; TATA-Box Binding Protein Associated Factor, RNA Polymerase I Subunit C; TAFI110; MGC:39976; TAFI95; SL1; TATA Box Binding Protein (TBP)-Associated Factor, RNA Polymerase I, C, 110kDa; TATA Box Binding Protein (TBP)-Associated Factor, RNA Polymerase I, C, 110kD; TATA Box-Binding Protein-Associated Factor RNA Polymerase I Subunit C; RNA Polymerase I-Specific TBP-Associated Factor 110 KDa; Transcription Initiation Factor SL1/TIF-IB Subunit C; TATA Box-Binding Protein-Associated Factor 1C; TBP-Associated Factor 1C; TATA-Box Binding Protein Associated Factor, RNA Polymerase I, C; Transcription Factor SL1; SL1, 110kD Subunit
Background

Gene Name: TAF1C

NCBI Gene Entry: 9013

Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human TAF1C 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 TAF1C-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.TAF1C 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 TAF1C and Hsp90 α, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using NaQ™ ECL Substrate Kit.
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RT-qPCR analysis. HT-1080 cells were infected with TAF1C-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.TAF1C 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 TAF1C and Hsp90 α, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using NaQ™ ECL Substrate Kit.
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