Site Directed Mutagenesis (SDM) Human Point mutation THP-1

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Get tips on using ON-TARGETplus Human SLC7A11 (23657) siRNA - SMARTpool to perform siRNA / miRNA gene silencing Human - BCBL-1 xCT

Products Dharmacon ON-TARGETplus Human SLC7A11 (23657) siRNA - SMARTpool

Get tips on using ON-TARGETplus Human ABCG2 (9429) siRNA - SMARTpool to perform siRNA / miRNA gene silencing Human - BCBL-1 BCR

Products Dharmacon ON-TARGETplus Human ABCG2 (9429) siRNA - SMARTpool

Get tips on using pET-21b(+)/Pro j 1 to perform Protein Expression Prokaryotic cells - E. coli Pro J 1

Products Mohammad-Ali Assarehzadegan, Department of Immunology, Faculty o pET-21b(+)/Pro j 1

Get tips on using Cell Proliferation Reagent WST-1 to perform Cell cytotoxicity / Proliferation assay cell type - SMMC-7721, Huh7, Hep3B, 293T

Products Sigma-Aldrich Cell Proliferation Reagent WST-1

Get tips on using Mouse SDF-1 α / CXCL12 α ELISA Kit to perform ELISA Mouse - SDF-1/CXCL12

Products Sigma-Aldrich Mouse SDF-1 α / CXCL12 α ELISA Kit

Get tips on using Mouse CXCL12/SDF-1 alpha Quantikine ELISA Kit to perform ELISA Mouse - SDF-1/CXCL12

Products R&D Systems Mouse CXCL12/SDF-1 alpha Quantikine ELISA Kit

The RNA-guided CRISPR-Cas9 nuclease system has revolutionized the genome editing practices. For the most part, the Cas9-mediated genome editing is performed either via nonhomologous end joining (NHEJ) or homology-directed repair (HDR) in mammalian cells, However, designing of specific sgRNAs and minimizing off-target cleavage mediated mutagenesis are the major challenges in CRISPR-Cas based genome editing. To circumvent these issues, we can take advantages of many available tools and approaches for sgRNA construction and delivery.

DNA CRISPR Mouse Deletion 3T3-L1 Trp53

ELISA is the most commonly used method of detecting and quantifying the concentration of an antigen in an unknown sample. During the experiment, If you get a weak signal, then make sure reagents are at room temperature before starting the assay. Try increasing incubation times to ensure maximal antibody binding and amplify the signal. Secondly, if you get values above 0 in the negative control indicates a high background signal. Try to consider reducing your antibody concentration and prevent non-specific binding of antibodies by using affinity-purified antibody and suitable blocking buffers. To avoid high well to well variation, do not stack plates during incubation, no bubbles in the plate and wash wells thoroughly to avoid variation.

Proteins ELISA Mouse SDF-1/CXCL12

Get tips on using GDNF RECEPTOR ALPHA 1 to perform Immunohistochemistry Mouse - GFRA1

Products Neuromics GDNF RECEPTOR ALPHA 1

Get tips on using CD31/PECAM-1 Antibody to perform Immunohistochemistry Mouse - CD31

Products Novus Biologicals CD31/PECAM-1 Antibody

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