Anti-ALG3 Aptamer(Cat#: CTApt-1144)
This product is an aptamer which binds to the ALG3 with an affinity of 1nM~1μM.
Specific Inquiry 
Summary
Specifications
| Target Category |
Protein |
| Target |
ALG3 |
| Alternative Names |
ALG3 Alpha-1,3- Mannosyltransferase; Dol-P-Man:Man(5)GlcNAc(2)-PP-Dol Alpha-1,3-Mannosyltransferase; NOT56L; Asparagine-Linked Glycosylation 3 Homolog (Yeast, Alpha-1,3-Mannosyltransferase) ; Dolichyl-Phosphate-Mannose--Glycolipid Alpha-Mannosyltransferase; Dolichyl-P-Man:Man(5)GlcNAc(2)-PP-Dolichyl Mannosyltransferase; Carbohydrate Deficient Glycoprotein Syndrome Type IV; Dol-P-Man-Dependent Alpha(1-3)-Mannosyltransferase; Asparagine-Linked Glycosylation Protein 3 Homolog; Not56-Like Protein; D16Ertd36e; CDGS4; Not56; Asparagine-Linked Glycosylation 3, Alpha-1,3- Mannosyltransferase Homolog (S. Cerevisiae) ; Asparagine-Linked Glycosylation 3 Homolog (S. Cerevisiae, Alpha-1,3-Mannosyltransferase) ; Asparagine-Linked Glycosylation 3, Alpha-1,3- Mannosyltransferase Homolog; Dol-P-Man Dependent Alpha-1,3- Mannosyltransferase; EC 2.4.1.130; EC 2.4.1.258; CDG1D; CDGS6; ALG3; Not; NOT |
| Gene ID |
10195 |
| UniProt ID |
Q92685 |
| Target Overview |
This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. |
| Chemical Modification |
DNA/RNA |
| Length |
20-80 nt |
| Affinity (Kd) |
1nM~1μM |
| Binding Conditions/Buffer |
PBS; buffer system with Serum; other |
For Research Use Only. Not for Diagnostic or Therapeutic Applications.
