ABclonal Technology

rRNA Depletion Kits (Plant) (ABclonal, Cat. RK30208) is a highly efficient rRNA removal kit specifically developed for angiosperms (leaf, seed, and root tissues). This kit is suitable for plant total RNA samples with a template amount of 10-1000 ng, effectively removing cytoplasmic rRNA (including cytoplasmic 5S rRNA, 5.8S rRNA, 18S rRNA, and 28S rRNA), plastid rRNA, and mitochondrial rRNA (including 12S rRNA and 16S rRNA) from total RNA through streptavidin magnetic bead adsorption.
The kit’s workflow consists of four main steps: hybridization of Ribo-Pools probes with target RNA, pre-treatment with streptavidin magnetic beads, rRNA removal, and RNA purification. The entire process can be completed within 60 minutes without the need for enzymatic digestion and is compatible with high-throughput automation. The kit does not rely on poly A selection and can be used for analyzing non-polyadenylated RNA, including non-coding RNA, histones, and whole transcriptome analysis.

rRNA Depletion Kits (Plant) (ABclonal, Cat. RK30208) is a highly efficient rRNA removal kit specifically developed for angiosperms (leaf, seed, and root tissues). This kit is suitable for plant total RNA samples with a template amount of 10-1000 ng, effectively removing cytoplasmic rRNA (including cytoplasmic 5S rRNA, 5.8S rRNA, 18S rRNA, and 28S rRNA), plastid rRNA, and mitochondrial rRNA (including 12S rRNA and 16S rRNA) from total RNA through streptavidin magnetic bead adsorption.
The kit’s workflow consists of four main steps: hybridization of Ribo-Pools probes with target RNA, pre-treatment with streptavidin magnetic beads, rRNA removal, and RNA purification. The entire process can be completed within 60 minutes without the need for enzymatic digestion and is compatible with high-throughput automation. The kit does not rely on poly A selection and can be used for analyzing non-polyadenylated RNA, including non-coding RNA, histones, and whole transcriptome analysis.

rRNA Depletion Kits (Plant) (ABclonal, Cat. RK30208) is a highly efficient rRNA removal kit specifically developed for angiosperms (leaf, seed, and root tissues). This kit is suitable for plant total RNA samples with a template amount of 10-1000 ng, effectively removing cytoplasmic rRNA (including cytoplasmic 5S rRNA, 5.8S rRNA, 18S rRNA, and 28S rRNA), plastid rRNA, and mitochondrial rRNA (including 12S rRNA and 16S rRNA) from total RNA through streptavidin magnetic bead adsorption.
The kit’s workflow consists of four main steps: hybridization of Ribo-Pools probes with target RNA, pre-treatment with streptavidin magnetic beads, rRNA removal, and RNA purification. The entire process can be completed within 60 minutes without the need for enzymatic digestion and is compatible with high-throughput automation. The kit does not rely on poly A selection and can be used for analyzing non-polyadenylated RNA, including non-coding RNA, histones, and whole transcriptome analysis.

The rRNA depletion module (H/M/R) is primarily designed for total RNA samples from humans, mice, and rats. It can effectively remove cytoplasmic rRNA (including cytoplasmic 5S rRNA, 5.8S rRNA, 18S rRNA, and 28S rRNA) and mitochondrial rRNA (including 12S rRNA and 16S rRNA) from total RNA. The resulting RNA can be used for library construction in Whole RNA-seq or other rRNA depletion analyses.
This product is suitable not only for total RNA samples with good integrity but also for degraded RNA samples, such as FFPE RNA. The required starting amount of total RNA is 10 ng to 1 μg.

The rRNA depletion module (H/M/R) is primarily designed for total RNA samples from humans, mice, and rats. It can effectively remove cytoplasmic rRNA (including cytoplasmic 5S rRNA, 5.8S rRNA, 18S rRNA, and 28S rRNA) and mitochondrial rRNA (including 12S rRNA and 16S rRNA) from total RNA. The resulting RNA can be used for library construction in Whole RNA-seq or other rRNA depletion analyses.
This product is suitable not only for total RNA samples with good integrity but also for degraded RNA samples, such as FFPE RNA. The required starting amount of total RNA is 10 ng to 1 μg.

The rRNA depletion module (H/M/R) is primarily designed for total RNA samples from humans, mice, and rats. It can effectively remove cytoplasmic rRNA (including cytoplasmic 5S rRNA, 5.8S rRNA, 18S rRNA, and 28S rRNA) and mitochondrial rRNA (including 12S rRNA and 16S rRNA) from total RNA. The resulting RNA can be used for library construction in Whole RNA-seq or other rRNA depletion analyses.
This product is suitable not only for total RNA samples with good integrity but also for degraded RNA samples, such as FFPE RNA. The required starting amount of total RNA is 10 ng to 1 μg.

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human)

application (WB, ELISA) & cross reactivity (Human)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Mouse)

application (WB, ELISA) & cross reactivity (Mouse)

application (WB, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse)

application (WB, ELISA) & cross reactivity (Human, Mouse)

application (WB, IHC-P, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Rat)

application (WB, ELISA) & cross reactivity (Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human, Mouse)

application (WB, ELISA) & cross reactivity (Human, Mouse)

application (WB, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IF/ICC, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human)

application (WB, ELISA) & cross reactivity (Human)

application (WB, IF-P, ELISA) & cross reactivity (Mouse, Rat)

application (WB, IF-P, ELISA) & cross reactivity (Mouse, Rat)

application (WB, ELISA) & cross reactivity (Mouse, Rat)

application (WB, ELISA) & cross reactivity (Mouse, Rat)

application (WB, ELISA) & cross reactivity (Human)

application (WB, ELISA) & cross reactivity (Human)

application (WB, ELISA) & cross reactivity (Mouse, Rat)

application (WB, ELISA) & cross reactivity (Mouse, Rat)

Ruby Bst DNA Polymerase is an in silico designed homologue of Geobacillus stearothermophilus DNA Polymerase I(large fragment). Ruby Bst DNA Polymerase has 5´→3´ DNA polymerase activity and strong strand displacement activity but lacks 5´→3´ exonuclease activity. Ruby Bst DNA Polymerase displays improved amplification speed, yield, salt tolerance and thermo stability compared with wild-type Bst DNA Polymerase, Large Fragment.

Ruby Bst DNA Polymerase is an in silico designed homologue of Geobacillus stearothermophilus DNA Polymerase I(large fragment). Ruby Bst DNA Polymerase has 5´→3´ DNA polymerase activity and strong strand displacement activity but lacks 5´→3´ exonuclease activity. Ruby Bst DNA Polymerase displays improved amplification speed, yield, salt tolerance and thermo stability compared with wild-type Bst DNA Polymerase, Large Fragment.

application (WB, ELISA) & cross reactivity (Mouse, Rat)

application (WB, ELISA) & cross reactivity (Mouse, Rat)

application (WB, ELISA) & cross reactivity (Mouse, Rat)

application (WB, ELISA) & cross reactivity (Mouse, Rat)