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Rnascope vs reagent kit red

Manufactured by Advanced Cell Diagnostics

The RNAscope® VS Reagent Kit - RED is a laboratory tool designed for the detection and visualization of target RNA molecules in tissue samples. The kit provides the necessary reagents to perform in situ hybridization, allowing researchers to localize and analyze the expression of specific RNA targets within the context of the tissue architecture.

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5 protocols using rnascope vs reagent kit red

1

Detecting TERT mRNA in FFPE Tissues

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mRNA ISH, a novel method to detect mRNA in FFPE tissues,26 (link) was performed for TERT mRNA on a Discovery Ultra automation system (Ventana Medical Systems, Inc.) by using RNAscope® VS Reagent Kit – RED (Advanced Cell Diagnostics). VS Probe – Hs-TERT (Cat#605516) specific to the sequence region between nucleotides 2164 to 3231 encoding the TERT transcript was used according to the manufacturer’s instructions. Briefly, 4-µm FFPE tissue sections of tumors were pretreated in citrate buffer with heat, followed by protease digestion before hybridization with the target oligo probes. Slides were hybridized sequentially with target probes incubated at 43°C for 2 h and 32 min, preamplifier at 53°C for 32 min, and amplifier at 53°C for 32 min, and label probes at room temperature for 12 min. Between the hybridization steps, slides were washed with Ribowash buffer (0.1× saline sodium citrate). Hybridization signals were detected by chromogenic development with Fast Red, followed by counterstaining with hematoxylin. Each sample was quality controlled for RNA integrity with an RNAscope probe for PPIB RNA and for background with a probe for bacterial dapB RNA. The specific RNA staining signal was identified as intracellular red punctate dots.
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2

Quantifying GH mRNA Expression

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In situ RNA hybridization was performed with RNAscope 2.5 HD Detection Reagent-RED and human GH1 probe (REF 539081) according to manufacturer protocols. Ubiquitous mRNA Mm-Ppib (REF 313911) was used as positive control, and bacterial RNA probe dabB (REF 310043) as negative control. Reagents were from Advanced Cell Diagnostics RNAscope VS Reagent Kit-RED. Paraffin tissue sections were de-paraffinized, dehydrated, and pretreated with RNAscope Pretreatment Kit to unmask target RNA and permeabilize cells. Tissue was hybridized with target-specific double Z human GH1 probe (corresponding to bases 77–825 of human GH1; GenBank accession #NM_000515.4). For GH mRNA expression, 9 samples in the young cohort, 10 in the middle-aged cohort, and 14 in the aged cohort were analyzed. Blinded analysis was performed to quantify GH mRNA cluster signals on a cell-by-cell basis by manual counting and percent positive cells per field (× 40) calculated in 3–8 fields for each specimen. Specimens from both sexes were analyzed together.
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3

Quantifying GH mRNA Expression

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In situ RNA hybridization was performed with RNAscope 2.5 HD Detection Reagent-RED and human GH1 probe (REF 539081) according to manufacturer protocols. Ubiquitous mRNA Mm-Ppib (REF 313911) was used as positive control, and bacterial RNA probe dabB (REF 310043) as negative control. Reagents were from Advanced Cell Diagnostics RNAscope VS Reagent Kit-RED. Paraffin tissue sections were de-paraffinized, dehydrated, and pretreated with RNAscope Pretreatment Kit to unmask target RNA and permeabilize cells. Tissue was hybridized with target-specific double Z human GH1 probe (corresponding to bases 77–825 of human GH1; GenBank accession #NM_000515.4). For GH mRNA expression, 9 samples in the young cohort, 10 in the middle-aged cohort, and 14 in the aged cohort were analyzed. Blinded analysis was performed to quantify GH mRNA cluster signals on a cell-by-cell basis by manual counting and percent positive cells per field (× 40) calculated in 3–8 fields for each specimen. Specimens from both sexes were analyzed together.
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4

In situ Hybridization of N40K mRNA in FFPE Tissues

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In situ hybridization for human N40K mRNA in formalin-fixed paraffin embedded (FFPE) tissues92 (link) was completed on a Discovery Ultra automation system platform (Ventana Medical Systems) using RNAscope® VS Reagent Kit – RED (Advanced Cell Diagnostics). An oligoprobe set specific for N40K (not for U1-70K) (Advanced Cell Diagnostics, Cat# 760-234) was applied according to the manufacturer’s instruction. Hybridization signals were detected by chromogenic development with Fast Red, followed by counterstaining with hematoxylin. Each sample was quality controlled for RNA integrity with RNAscope oligoprobes for PPIB RNA, and for non-specific background staining with oligoprobes for bacterial dapB RNA. The specific RNA staining signal was identified as intracellular red punctate dots.
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5

Detecting TERT mRNA in FFPE Tissues

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mRNA ISH, a novel method to detect mRNA in FFPE tissues,26 (link) was performed for TERT mRNA on a Discovery Ultra automation system (Ventana Medical Systems, Inc.) by using RNAscope® VS Reagent Kit – RED (Advanced Cell Diagnostics). VS Probe – Hs-TERT (Cat#605516) specific to the sequence region between nucleotides 2164 to 3231 encoding the TERT transcript was used according to the manufacturer’s instructions. Briefly, 4-µm FFPE tissue sections of tumors were pretreated in citrate buffer with heat, followed by protease digestion before hybridization with the target oligo probes. Slides were hybridized sequentially with target probes incubated at 43°C for 2 h and 32 min, preamplifier at 53°C for 32 min, and amplifier at 53°C for 32 min, and label probes at room temperature for 12 min. Between the hybridization steps, slides were washed with Ribowash buffer (0.1× saline sodium citrate). Hybridization signals were detected by chromogenic development with Fast Red, followed by counterstaining with hematoxylin. Each sample was quality controlled for RNA integrity with an RNAscope probe for PPIB RNA and for background with a probe for bacterial dapB RNA. The specific RNA staining signal was identified as intracellular red punctate dots.
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