siRNA / miRNA gene silencing Human SPC-A1

- Found 5917 results

miRNeasy Mini kit Product

Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Cells - primary hematopoietic stem cells

Products Qiagen miRNeasy Mini kit
SNP Type™ 96.96 Genotyping Reagent Kit with Control Line Fluid—10 IFCs Product

Get tips on using SNP Type™ 96.96 Genotyping Reagent Kit with Control Line Fluid—10 IFCs to perform Cell line authentication Human prostatic cancer cell line DU145

Products Fluidigm SNP Type™ 96.96 Genotyping Reagent Kit with Control Line Fluid—10 IFCs
SNP Type™ 96.96 Genotyping Reagent Kit with Control Line Fluid—10 IFCs Product

Get tips on using SNP Type™ 96.96 Genotyping Reagent Kit with Control Line Fluid—10 IFCs to perform Cell line authentication Human prostatic cancer cell line PC3

Products Fluidigm SNP Type™ 96.96 Genotyping Reagent Kit with Control Line Fluid—10 IFCs
miRNeasy Mini kit Product

Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Cells - primary rat lymph node cells

Products Qiagen miRNeasy Mini kit
DMEM–Dulbecco's Modified Eagle Medium Product

Get tips on using DMEM–Dulbecco's Modified Eagle Medium to perform Mammalian cell culture media A172

Products Thermo Fisher Scientific DMEM–Dulbecco's Modified Eagle Medium
RNA isolation / purification Bacteria - Gram positive Staphylococcus aureus Experiment

The challenge in isolating RNA from S. aureus cells is the disruption of the cell wall. A lot of protocols employ enzymatic digestion (pretreatment) which may affect gene expression patterns of certain genes. Therefore physical disruption using beads is considered to be the better alternative.

RNA RNA isolation / purification Bacteria Gram positive Staphylococcus aureus
RNA isolation / purification Bacteria - Gram positive Streptococcus pneumoniae Experiment

The biggest problem in isolating RNA from gram-positive bacteria is the disruption of the cell wall. A lot of protocols employ enzymatic digestion (pretreatment) which may affect gene expression patterns of certain genes. Therefore physical disruption using beads could be the best alternative.

RNA RNA isolation / purification Bacteria Gram positive Streptococcus pneumoniae
RNA isolation / purification Bacteria - Gram positive Mycobacterium tuberculosis Experiment

The biggest problem in isolating RNA from gram-positive bacteria is the disruption of the cell wall. A lot of protocols employ enzymatic digestion (pretreatment) which may affect gene expression patterns of certain genes. Therefore physical disruption using beads can be a best alternative.

RNA RNA isolation / purification Bacteria Gram positive Mycobacterium tuberculosis
RNA isolation / purification Bacteria - Gram positive Enterococcus faecalis Experiment

The biggest problem in isolating RNA from gram-positive bacteria is the disruption of the cell wall. A lot of protocols employ enzymatic digestion (pretreatment) which may affect gene expression patterns of certain genes. Therefore physical disruption using beads can be a best alternative.

RNA RNA isolation / purification Bacteria Gram positive Enterococcus faecalis
RNA isolation / purification Bacteria - Gram positive Bacillus anthracis Experiment

The biggest problem in isolating RNA from gram-positive bacteria is the disruption of the cell wall. A lot of protocols employ enzymatic digestion (pretreatment) which may affect gene expression patterns of certain genes. Therefore physical disruption using beads can be a best alternative.

RNA RNA isolation / purification Bacteria Gram positive Bacillus anthracis

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