siRNA synthesis-in vivo

siRNA is a double strand RNA that is 20 to 25 nucleotides. After transfection of siRNA into the cell, it will cause knockdown of its specific gene.

Biotools provides customized siRNA design and synthesis. We also provide customized siRNA set, which guarantees at least 70% knockdown efficiency.

Features
● Free siRNA design
● High stability and long effect
● Guarantee at least 70% knockdown efficiency for sets

 

siRNA

Chemically modified siRNA

in vitro stability

weak

strong

Reaction time

shorter, 1 week

Longer, 2 weeks

in vivo activity

weak

strong

Reproducibility

high

higher


All you need to do is to provide the gene sequence or NCBI number, we will design and choose the siRNA that has the best knockdown effect. 

Product specification

siRNA

Product Price(USD)
in vivo siRNA 2OD/4OD 366.67 / 550
Negative control siRNA 1OD 83.33
FAM labeled negative control siRNA  
Positive control siRNA  
 

siRNA set 

siRNA set Price
  3 x 2 OD target siRNA
  1 OD negative control siRNA
  1 OD FAM labeled negative control siRNA
  1 OD positive control siRNA
733.33

*Guaranteed>70% knock-down in mRNA level




Working  day not including delivery time: 2 weeks
1. Please provide the accurate gene ID, species or gene sequence
2. Please confirm product specificity
  • Jung-Lin Wu, Hsin-Yi Wu, Kuo-I Lin, et al., Temporal regulationof Lsp1 O-GlcNAcylation and phosphorylation during apoptosis ofactivated B cells. nature communications, 2016.

  • *Shu-Yi Yin, Feng-Yi Jian, Ning-Sun Yang, et al., Induction of IL-25 secretion form tumor-associated fibroblasts suppresses mammary tumor metastasis. nature communications, 2016.                                                                                                                                                                                                         
  • Lin LP, Yu TY, Chang HN, Tsai WC, Pang JS. Simvastatin Downregulates Cofilin and Stathmin to Inhibit Skeletal Muscle Cells Migration. Int J Mol Sci. 2022 Mar 5;23(5):2848.
Q1.  Is there any difference in the negative control of normal and chemically-modified siRNA?
A:  The sequence is the same, but there will be a chemical modification for the siRNA in our chemically-modified set

Q2.  How do you check the off-target effect of siRNA?
A:  We will avoid this situation when we first design the sequence but the customer must check

Q3.  What is the highest concentration for siRNA? Can we pool the 3 siRNAs together?
A:  The most we suggest is 4 times more than our recommendation, and we do not suggest you pool the 3 siRNAs together

Q4.  Can you evaluate the knockdown efficiency when designing siRNA sequence?
A:  No. The knockdown efficiency depends on the cell type

Q5. ​ Where is the exact location of the chemical modification at siRNA?
A: ​Depends on what type of modification. For O-Me, it will be on the 2' of every ribonucleotide