Western Blot data demonstrating successful knockdown of p53 in human cells 48 hours after treatment with QX33 siRNA and IFN gamma(SC = Scrambled Control (Product Number QC1), siRNA = QX33 treatment)
Western Blot data demonstrating successful knockdown of p53 in human cells 48 hours after treatment with QX33 siRNA and IFN gamma(SC = Scrambled Control (Product Number QC1), siRNA = QX33 treatment)

TranslationBlocker Human IRF1 siRNA

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Human IRF1 siRNA Translation Blocker™ Duplex

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Datasheets and Documentation
Product Datasheet
SKU: QX33-2nmol

Human IRF1 TranslationBlocker™ siRNA Duplex Product Attributes

Blocks transcription and translation of IRF1 from: Human.
May also react with IRF1 based upon sequence homology and clone specific publications.
Type of RNAi: siRNA.
siRNA target sequence: NM_002198.
Samples and cell lines tested: U-2 OS Huan Osteosarcoma Epithelial Cells from Bone.
Buffer and Stabilizer: Lyophilized. See datasheet for resuspension instructions and buffer information.
Concentration of Anti-Human IRF1: Lyophilized
SiRNA Purification Method:RPC/HPLC
Storage Conditions: Store Lyophilized siRNA duplex at 4C. Reconsituted product may be stored at -20C for up to 1 month.
    IRF1 Knockdown Protocol:
    1. Starting with cultured cells in growth media seed plates with cells and incubated at 37°C. For example, seed 12 well plates with 1x105 cells and incubate at 37°C until cells reach 70% confluence prior to starting transfections
    2. Prepare transfection reagent in serum-free growth medium such as Opti-MEM-I. Allow to come to room temperature. Lipofectamine 2000 was used to generate the above data in accordance with manufacturer’s instructions. li>
    3. Dilute siRNA to working concentration in serum-free growth media. For Lipofectamine or similar transfections into 12 well plates, we recommend starting siRNA dose optimization at around 100 pmol siRNA duplex.Optimal dilution should be experimentally determined.
    4. Combine diluted siRNA and transfection reagent. Ratio of transfection reagent to siRNA should be optimized. Equivalent volumes of prepared Lipofectamine 2000 or other transfection reagent and diluted siRNA should be combined and incubated at room temperature for 30 minutes with gentle mixing (optional).
    5. Add prepared siRNA solution to cells. For 12 well plates this will entail adding the solution to cells in approximately 1.1 ml serum-free medium. Optionally, FITC labeled control siRNA (Product Number QC-1F) or positive control siRNA (Beta-Actin; Product Number QC-2) may be used to assess transfection efficiency.
    6. Incubate for several hours in serum free media. Typically, 4 hour incubation is recommended for this initial transfection step.
    7. Add serum containing media to culture without a media change if longer incubation times are required. The above data required an additional 48 hour incubation to examine IFN gamma (interferon gamma) induction of a response (1000 U/ml). Generally 1-2 fold of the original volume of siRNA containing serum-free media is added to restore nutrient levels in media. Alternatively, the media may be directly supplemented with serum such as 10% FBS.
    8. Incubate and assay several hours after transfection. Optimal knockdown time should also be experimentally determined. Optionally, a second transfection can be performed 24 hours after the first transfection to enhance knockdown. Interferon Regulatory Factor 1 (IRF1) knockdown at the protein level was measured at 48 hours post transfection via Western Blot.

IRF1 General Information

Gene Name: IRF1
Entrez Gene ID: 3659
NCBI Ref Seq Accession Number: NP_002189
Uniprot ID:
IRF1 Molecular Weight:
Alternate Names: IRF-1, Interferon Regulatory Factor 1, MAR

Limitations and Warranty

This product is for Research Use Only. This product is guaranteed to work for a period of two years when stored at -70C or colder, and one year when aliquoted and stored at -20C.

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TranslationBlocker Human IRF1 siRNA

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