| Product |
Cat No. |
Details |
Size |
Link |
 |
Benzonase Nuclease |
SB-G3461-50KU |
- This endonuclease can attack and degrade all forms of DNA and RNA under very broad conditions
- Can effectively reduce the viscosity of protein lysates such as cells, tissues and microorganisms
- Purity: ≥95% by SDS-PAGE, no protease, ≥250 U/μL
|
200 ul |
 |
|
Benzonase Nuclease (His tag) |
SB-G3406-50KU |
- This endonuclease can attack and degrade all forms of DNA and RNA under very broad conditions
- Can effectively reduce the viscosity of protein lysates such as cells, tissues and microorganisms
- Has his - tag, which can be removed by nickel column absorption
- Purity: ≥95% by SDS-PAGE, no protease, ≥250 U/μL
|
50 KU |
|
 |
Bst DNA polymerase, Large Fragment |
SB-G3403-1600U |
- Mainly used in isothermal amplification reactions, such as LAMP (Loop-mediated isothermal amplification), RCA (Rolling-circle amplification), etc
- Source : The large fragment derived from Bacillus stearothermophilus DNA polymerase I
- Purity and concentration : SDS-PAGE detection purity ≥ 95%
|
1600 U |
|
 |
DNA polymerase I (E. coli) |
SB-G3478-500U |
- In the presence of templates and primers (DNA or RNA), dNTPs are used as substrates to synthesize DNA complementary to the template along the 5'-3' direction. The enzyme also retains double-strand specific 5'-3' exonuclease activity and single-strand specific 3'-5' exonuclease activity
- Source : derived from Escherichia coli
- Purity and concentration: SDS-PAGE detection purity ≥ 95%
|
500 U |
|
 |
DNA polymerase I, Large (Klenow) Fragment |
SB-G3457-100U |
- Mainly used for the blunt end of the 5' or 3' protruding end of double-stranded DNA, 5' end labeling, Sanger dideoxy method for DNA sequencing, cDNA second-strand synthesis, site-directed mutagenesis, etc
- Source : derived from Escherichia coli
- Purity and concentration: SDS-PAGE detection purity ≥ 95%
|
100 U |
|
 |
DNA Topoisomerase I (Vaccinia Virus) |
SB-G3401-1000U |
- Features: DNA unwinds supercoils and specifically opens the connecting phosphodiester bonds
- Source: Escherichia coli strain carrying Vaccinia virus topoisomerase gene
- Purity and concentration: SDS-PAGE detection purity ≥ 95%
|
1000 U |
|
 |
dsDNase (Thermolabile) |
SB-G3408-50UL |
- Specifically cleaves the phosphate diester bond in double stranded DNA to produce oligonucleotides with 5 ' -phosphate and 3 ' -hydroxyl ends
- Source : Shremp derived deoxyribonuclease
- Purity : SDS-PAGE detection purity ≥ 95%
|
50 ul |
|
 |
Exonuclease I (E. coli) |
SB-G3464-3000U |
- Degrades single-stranded DNA in the 3'-5' direction, and decomposes to generate 5'-mononucleotides
- Source : derived from Escherichia coli
- Purity and concentration : SDS-PAGE detection purity ≥ 95%; 20 U/μL
|
3000 U |
|
 |
Exonuclease III (E.coli) |
SB-G3465-5000U |
- Mainly used for single-strand template preparation, site-directed mutagenesis, and strand-specific probe preparation for DNA dideoxy sequencing
- Source : derived from Escherichia coli
- Purity and concentration : SDS-PAGE detection purity ≥ 95%; 100 U/μL
|
5000 U |
|
 |
Fast Taq DNA polymerase |
SB-G3442-1000U |
- Taq DNA polymerase mutant obtained through in vitro evolutionary screening based on wild-type Taq DNA polymerase
- Source : derived from Thermus aquaticus
- Purity and concentration: SDS-PAGE detection purity ≥ 95%
|
1000U |
|
 |
Fast High Fidelity DNA polymerase |
SB-G3444-200U |
- Engineered ultra-high fidelity DNA polymerase combining with single-stranded DNA-binding protein
- Purity and concentration: ≥ 95% detected by SDS-PAGE
- Concentration：2 U/μL
|
200U |
|
 |
M-MLV Reverse Transcriptase |
CSB-DEM025 |
- Genetically engineered Reverse Transcriptase, which reduces the activity of RNase H and
improves the thermal stability
- Purity: 90%±5% by SDS-PAGE
- Shape: Liquid
- Application: RT-PCR, qPCR, qRT-PCR
- Source: MicroorganismEC No.:EC 2.7.7.49
|
10000U |
|
 |
mRNA Cap 2´-O-Methyltransferase |
SB-G3455-2000U |
- Can add a methyl group to the 2'-O position of the first nucleotide adjacent to the cap structure at the 5' end of the RNA to form a Cap-1 structure
- Source: derived from vaccinia virus
- Purity and concentration: SDS-PAGE detection purity > 95%
|
2000U |
|
 |
Poly(A) Polymerase |
SB-G3453-500U |
- Catalyzes the addition of AMP converted from ATP to the 3' end of single-stranded RNA in a template-independent manner to form a Poly(A) tail
- Source: derived from Escherichia coli
- Purity and concentration: SDS-PAGE detection purity > 95%
|
500U |
|
 |
Phi29 DNA polymerase |
SB-G3448-300U |
- Has DNA strand replacement activity and strong DNA continuous synthesis ability
- Source : DNA Polymerase gene derived from Bacillus subtilis phage phi29
- Purity and concentration: SDS-PAGE detection purity ≥ 95%
|
300U |
|
 |
RecQ DNA Helicase, Recombinant (100µg) |
FNK-01-004 |
- Studies on mechanisms of DNA recombination, replication and repair
- Application for genetic engineering. For dissociation of special structure DNA
- Biochemical Activities Unwinding duplex DNA, dependent on ATP. DNA-dependent ATPase
- Purity Over 90% by SDS-PAGE (CBB staining)
- Protein concentration 0.5 mg/ml as measured by BCA method
|
100 µg |
|
|
Ribonuclease R (RNase R) |
SB-G3462-500U |
- Mainly used for gene expression and variable splicing research, enriching circular RNA or lariat RNA
- Source : derived from Escherichia coli
- Purity and concentration : SDS-PAGE detection purity ≥ 95%; 20 U/μL
|
500U |
|
 |
Recombinant DNase I (RNase-free) |
SB-G3342-500U |
- Features: specifically degrades DNA, but cannot degrade RNA
- Source: Recombinant expression of the pichia coli strain carrying the Bovine Pancreatic DNase I gene
- Purity: SDS-PAGE purity ≥95%, RNase free; 10 U/mu L
|
500U |
|
| SB-G3342-10KU |
10KU |
|
 |
Recombinant RNase A (10 mg/mL) |
SB-G3405-200UL |
- Used to prepare DNA without host RNA; Can minimize the risk of pathogen introduction into the bioprocess
- Origin: Pancreas RNase A gene from Bovine pancreas
- Purity and concentration:The purity is ≥95% by SDS-PAGE
|
200UL |
|
| SB-G3405-1ML |
1ML |
|
 |
RecQ DNA Helicase, Recombinant |
FNK-01-003 |
- Studies on mechanisms of DNA recombination, replication and repair
- Application for genetic engineering. For dissociation of special structure DNA
- BiochemicalActivities Unwinding duplex DNA, dependent on ATP. DNA-dependent ATPase
- Purity Over 90% by SDS-PAGE (CBB staining)
- Protein concentration 0.5 mg/ml as measured by BCA method
|
20 µg |
|
|
RNase H (E.coli) |
SB-G3417-100U |
- Mainly used to remove mRNA before the second strand of cDNA is synthesized, remove poly(A) in mRNA hybridized with poly(dT), and achieve fixed-point shearing of RNA through DNA sequence, etc
- Source : derived from Escherichia coli
- Purity and concentration : SDS-PAGE detection purity ≥ 95%; 2 U/μL
|
100 U |
|
|
SweScript Reverse Transcriptase I |
SB-G3415-10KU |
- Has no RNase H activity, avoiding the degradation of RNA in the DNA/RNA hybrid template in the first-strand cDNA synthesis reaction, thereby ensuring the amount and length of the first-strand cDNA synthesis; compared with the wild-type enzyme
- Source : derived from M-MLV (Moloney Murine Leukemia Virus)
- Purity and concentration: SDS-PAGE detection purity ≥ 95%
|
10 KU |
|
|
SweScript Reverse Transcriptase II |
SB-G3416-10KU |
- Has no RNase H activity, avoiding the degradation of RNA in the DNA/RNA hybrid template in the first-strand cDNA synthesis reaction, thereby ensuring the amount and length of the first-strand cDNA synthesis; compared with the wild-type enzyme
- Thermal stability and synthesis efficiency are further improved
- Source : derived from M-MLV (Moloney Murine Leukemia Virus)
- Purity and concentration: SDS-PAGE detection purity ≥ 95%
|
10 KU |
|
 |
T4 DNA Polymerase |
SB-G3456-150U |
- Mainly used for blunt-ended DNA 5' or 3' protruding ends, labeled DNA probe synthesis, site-directed mutagenesis, etc.
- Source : derived from the recombinant expression of T4 bacteriophage in Escherichia coli
- Purity and concentration: SDS-PAGE detection purity > 95%
|
150 U |
|
 |
T4 Polynucleotide Kinase |
SB-G3458-500U |
- Mainly used for DNA and RNA 5' end labeling and 5' end phosphorylation of synthetic DNA linkers
- Source: Derived from T4 bacteriophage
- Purity and concentration: SDS-PAGE detection purity ≥ 95%
|
500 U |
|
 |
T5 Exonuclease |
SB-G3463-1000U |
- Exonuclease that degrades double-stranded or single-stranded DNA in the 5'→3' direction
- Source : Derived from T5 phage
- Purity and concentration : SDS-PAGE detection purity ≥ 95%; 10 U/μL
|
1000 U |
|
 |
Taq DNA Polymerase |
SB-G3441-1000U |
- Applications: Ideal for routine PCR applications, TA cloning
- Source : E.coli cells with a cloned polA gene from Thermus aquaticus
- Concentration: 5 U/μL
|
1000 U |
|
 |
Terminal Deoxynucleotidyl Transferase |
SB-G3412-50UL |
- Applications: Synthesis of homopolymers and heteropolymers
- Source : Recombinant expression in Escherichia coli strain carrying calf thymus gene
- Purity and concentration : SDS-PAGE detection purity ≥ 95%
|
50 ul |
|
|
Thermostable RNase H |
SB-G3418-250U |
- Mainly used to remove mRNA before the second strand of cDNA is synthesized, remove poly(A) in mRNA hybridized with poly(dT), and realize the fixed point of RNA through DNA sequence cut etc.
- Source : derived from thermophilic bacteria
- Purity and concentration : SDS-PAGE detection purity ≥ 95%; 5 U/μL
|
250 U |
|
|
Uracil-DNA Glycosylase (UDG) |
CSB-DEM026 |
- Application: Removal of uracil bases from single or double stranded DNA, Control of carry-over contamination in PCR
- Source: Recombinant in E.coli
- Active: 5U/μL
|
1000 U |
|
|
Uracil-DNA Glycosylase (UDG) |
SB-G3419-1000U |
- Mainly used to eliminate the product contamination problem during PCR amplification
- Source : derived from Escherichia coli,
- Purity and concentration : SDS-PAGE detection purity ≥ 95%; 5 U/μL
|
1000 U |
|
