Custom RNA Oligos

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Overview

RNA oligos, short for ribonucleic acid oligonucleotides, are single-stranded synthetic RNA sequences that can serve as an important regulator of gene function analysis and development of novel therapeutic strategies. With precise customization options, researchers can design RNA oligos with specific sequences to target and manipulate gene expression, study RNA structure and function, or develop therapeutic interventions for diseases. Additionally, RNA oligos can be chemically modified to enhance stability, specificity, or delivery efficiency in experimental settings.

Tsingke provides high-quality and cost-effective custom RNA oligos with various synthesis types and specific modifications to meet researchers' different needs, facilitating advancements in gene editing, germplasm transformation, genetic regulation, etc. To ensure product qualification, all RNA oligos use high-quality raw materials and synthesis processes, are purified by OPC or HPLC methods, and are 100% mass spectrometrically detected. We address challenges such as low coupling efficiency between bases, product decomposition susceptibility, demanding operating environments, and high costs, providing reliable solutions for your research needs.

Advantages
Various Product Types
Various RNA synthesis products, such as sgRNA, siRNA, miRNA, etc.
Rapid Synthesis Cycle
Regular orders can be completed in 3-4 days
Various QC Methods
100% mass spectrometry with a variety of additional detection options
Service Details

Name

Type

Quantity

Purification

Turnaround Time
(Bussiness Day)

QC

Modification

sgRNA

sgRNA

1.5 nmol

OPC

7

Mass Spectrometry

Add specific modifications 

1.5 nmol

HPLC 

12~15

Mass Spectrometry

HPLC

crRNA

crRNA

5 nmol /2 OD

HPLC 

12~15

Mass Spectrometry

HPLC

siRNA Oligo Duplex

1 siRNA 

5 nmol /2 OD

HPLC

3~4

Mass Spectrometry

HPLC

/

siRNA NC

2.5 nmol /1 OD

Available in stock

/

3 siRNA, 1 Guaranteed

5 nmol /2 OD

3~4

3 unique siRNA duplexes/FAM labeled NC  
(1 nmol)/Negative and Positive control
(2.5 nmol each)

At least one guaranteed gene knockdown (≥70%)

4 siRNA, 1 Guaranteed

5 nmol /2 OD

3~4

4 unique siRNA duplexes/1 FAM labeled NC
(1 nmol)/Negative and Positive control (2.6 nmol each)

At least one guaranteed gene knockdown (≥70%)

miRNA

miRNA mimics

5 nmol/2 OD

HPLC

3~4

Mass Spectrometry

HPLC

/

miRNA inhibitor

10 nmol/2 OD

mimics/
inhibitor(NC)

1 OD

Available in stock

miRNA agomir

2 OD

5~7

miRNA antagomir

2 OD

agomir/antagomir (NC)

2 OD

ASO

PS-ASO

2 OD

HPLC

3~4

Mass Spectrometry

HPLC

/

LNA-ASO

2 OD

OMe-ASO

2 OD

Workflow
High-throughput synthesizer from pmol to mmol levels
Synthesis
High-throughput synthesizer from pmol to mmol levels
Waters 2695 & Waters 2767 automatic purification and HPLC purification
Purification
Waters 2695 & Waters 2767 automatic purification and HPLC purification
Mass quality inspection, HPLC and other additional quality inspections
QC
Mass quality inspection, HPLC and other additional quality inspections
Automatic dispensing instrument for accurate dispensing
Distribution
Automatic dispensing instrument for accurate dispensing
Tube or Customized、Lyophilized RNA、COA Report
Delivery
Tube or Customized、Lyophilized RNA、COA Report
Case
Figure 1: Molecular weight deviation ≤ 0.05%
             
Figure 2: HPLC: Purity = 97.29%
Related Resource
FAQ
After transfection, no fluorescence is observed?

Usually, FAM shows green fluorescence after transfection and CY3 shows red fluorescence after transfection. When observing, first confirm whether the fluorescence excitation wavelength is correct, the green light wavelength is 495 nm and the red light is 550 nm.

After transfection, you need to wash immediately to observe the fluorescence and avoid too long time.

If the product is not stored properly, siRNA will be degraded and FAM will be quenched. FAM is easily decomposed by light, so please store it away from light.

When transfecting, operate away from light and avoid exposing FAM to white light for a long time.

Transfection time is too long, and fresh medium is not replaced in time after transfection.

A lot of cell death after transfection?

Poor cell status, need to adjust cell growth status: generally cells in good growth status have better tolerance to transfection reagents; siRNA or transfection reagent concentration is too high; transfection reagent is more toxic, replace transfection reagent; siRNA purity is low, impurities affect cell status; transfection time is too long, not timely replacement of fresh medium after transfection.

Low efficiency of cell transfection?

siRNA purity is too low, pay attention to lysis, avoid RNA enzyme contamination, use consumables and reagents treated by DEPC; siRNA transfection reagent complex concentration is low, need to optimize transfection efficiency, use appropriate transfection reagent dose; serum affects transfection efficiency, when preparing the mixture, it should not contain serum; culture can have serum, but do not have Antibiotics; 

Precautions for using siRNA

The product is shipped in the form of lyophilized powder, the dry powder is attached to the wall of the tube and is easily dispersed when opened, so please centrifuge the tube for a few seconds before dilution to make the product gather at the bottom of the tube and open the cap carefully, cover the tube after dissolution, vortex and shake to mix to make full dissolution. It is recommended to store at -20 ℃ or below, avoid repeated freezing and thawing, and keep in separate containers. Centrifuge instantly before use and prepare 20 μm-100 μm storage solution with RNase-free Water or ddH2O, the average molecular weight of siRNA is 13300. RNA handling rules should be strictly followed and RNase-free lab supplies should be used for experimental operations to avoid degradation of RNA. Please keep on ice when using this product. For RNA with fluorescent marker, we use brown centrifuge tube to pack, because the fluorescent marker is sensitive to light, it must be stored away from light.

**For Research Use Only. Not for use in diagnostic procedures.
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