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Human LAMB1 Knockdown Cell Line (Wb-Validated) #C65445

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RT-qPCR analysis. HeLa cells were infected with LAMB1-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.LAMB1 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 LAMB1 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:
    LAMB1
  • 货号:
    C65445
  • 应用:
  • 物种反应性:
规格:
1 Kit
价格:
询价
Information
Product Name Human LAMB1 Knockdown Cell Line (Wb-Validated)
Aliases LAMB1; Laminin Subunit Beta 1; Laminin Subunit Beta-1; Laminin B1 Chain; Laminin, Beta 1; CLM; Cutis Laxa With Marfanoid Phenotype; Laminin-10 Subunit Beta; Laminin-12 Subunit Beta; Laminin-1 Subunit Beta; Laminin-2 Subunit Beta; Laminin-6 Subunit Beta; Laminin-8 Subunit Beta; LIS5
Background

Gene Name: LAMB1

NCBI Gene Entry: 3912

Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human LAMB1 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 LAMB1-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.LAMB1 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 LAMB1 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. HeLa cells were infected with LAMB1-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.LAMB1 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 LAMB1 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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