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Human MYD88 Knockdown Cell Line (Wb-Validated) #C62307

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RT-qPCR analysis. HT-1080 cells were infected with MYD88-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. MYD88 protein expression in wild-type (WT) and shRNA knockdown (KD) HT-1080 cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against MYD88 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：

MYD88
货号：

C62307
应用：
物种反应性：

规格：

1 Kit

价格：

询价

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Product Name	Human MYD88 Knockdown Cell Line (Wb-Validated)
Aliases	MYD88 Innate Immune Signal Transduction Adaptor; Myeloid Differentiation Primary Response Protein MyD88; Myeloid Differentiation Primary Response Gene (88); Myeloid Differentiation Primary Response 88; TLR Adaptor MYD88; Mutant Myeloid Differentiation Primary Response 88; MYD88D; IMD68; WM1
Background	Gene Name: MYD88 NCBI Gene Entry: 4615
Storage	Store at liquid nitrogen for 1 year.
Kit Components	1. Human MYD88 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 MYD88-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. MYD88 protein expression in wild-type (WT) and shRNA knockdown (KD) HT-1080 cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against MYD88 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)

基因名：

MYD88
货号：

C62307
应用：
物种反应性：

规格：

1 Kit

价格：

询价

Datasheet

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