PDGF-AB (Platelet-derived growth factor-AB) is an important member of the platelet-derived growth factor (PDGF) family. It belongs to heterodimeric proteins, formed by the dimerization of PDGFA and PDGFB subunits. It is a class of extracellular signaling molecules with diverse biological activities, widely involved in various physiological and pathological processes of the body. The structural core of PDGF-AB consists of two subunits (α and β) linked by disulfide bonds to form a stable protein structure. Distinct from the homodimers of the PDGF family (such as PDGF-AA and PDGF-BB), its structural characteristics determine the uniqueness of its receptor binding specificity and biological functions. It can specifically bind to PDGF receptors (PDGFR) on the cell surface and initiate downstream signaling pathways.
This product is provided as a lyophilized powder, featuring high activity, high purity, low endotoxin, high stability, and no tag.
Product Information
|
Product Information. |
Catalog Number |
Size |
|
Recombinant Human PDGF-AB Protein |
91618ES10 |
10 μg |
|
91618ES50 |
50 μg |
|
|
91618ES80 |
1 mg |
Performance Parameters
|
Synonyms |
Platelet-derived Growth Factor AB; PDGFAB |
|
Species |
Human |
|
Source |
CHO Cells |
|
Sequence |
Human PDGF-A(Ser87-Thr211)&Human PDGF-B(Ser82-Thr190) |
|
Accession |
P04085&P01127 |
|
Tag |
Tag Free |
|
Molecular Weight |
Predicted molecular mass:14.3 kDa&12.3 kDa |
|
Endotoxin |
≤10 EU/mg by the LAL method |
|
Purity |
≥95%, by SDS-PAGE (under reducing (R) & Non-reducing conditions, visualized by Coomassie staining) |
|
Activity |
Measure in a cell proliferation assay using NIH3T3 cells. The ED50 is ≤1.0 ng/mL. |
|
Formulation |
PBS, 5% Mannitol and 0.01% Tween 80, pH7.4. |
|
Appearance |
Lyophilized Powder |
Storage
Store at -25~-15°C. Valid for 1 year from the date of receipt. After reconstitution, store at 2~8°C for 7-10 days. After reconstitution, store at -85~-65°C for up to 6 months.
Reconstitution Method
Reconstitute the lyophilized protein with sterile deionized water. It is recommended to aliquot the protein upon first use to avoid repeated freeze-thaw cycles.
Notes
1. For your safety and health, please wear a lab coat and disposable gloves during operation.
2. This product is for research use only.
Documents:
Manuals
91618_Manual_HB20260408
Citation
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Discription:
- This product is a type IIS restriction endonuclease derived from the recombinant protein encoded by the BsaI gene in Bacillus sphaericus expressed by E.coli. Its recognition sequence is 5'-GGTCTCN1/N5-3'. Use to digest plasmids to prepare poly(A/T/G/C)-terminated linearized DNA fragments to obtain specific cohesive ends.
This product is produced in accordance with GMP process requirements and provided in a liquid form.
Applications
Specifications
Expression Host | Recombinant E. coli with Bas I gene | |
Reaction Temperature | 37℃ | |
Storage Buffer | 10mM Tris-HCl, 0.2M NaCl, 0.1mM EDTA, 1mM DTT, 50% Glycerol, 0.2mg/ml OsrHSA pH 7.4±0.2 (25℃) | |
Unit Definition | 1 unit: The amount of enzyme required to digest 1 μg of substrate DNA within 1 h at 37℃ in a 50 μL system. | |
Application | 1.Digest the plasmid to prepare a linearized DNA fragment at the end of Poly (A/T/C/G); 2.Digestion of DNA to obtain specific sticky ends; 3.Linearize plasmid template before in-vitro transcription. |
Components
Components No. | Name | 10661ES03 | 10661ES10 | 10661ES60 |
10661 | Bsa I GMP-grade (20 U/μL) | (1 KU)
| (10 KU) | (100 KU) |
Shipping and Storage
This product should be stored at -25 ~ -15℃ for two years.
Description

Figure1. No non-specific nuclease residues test
20 U BsaI was incubated with substrate DNA at 37°C for 1 h and 16 h, and DNA band changes were compared by agarose gel electrophoresis. The results showed that there was no non-specific nuclease residue in BsaI.

Figure2. The end integrity is good and the effect is consistent with imported brands
When BsaI and substrate DNA were incubated in the enzyme digestion reaction system for 16 hours at 37°C, no non-specific degradation of the substrate caused by star activity was detected, indicating that there was no star activity after 16 hours of incubation with BsaI.
FAQ

Figure1. No non-specific nuclease residues test
20 U BsaI was incubated with substrate DNA at 37°C for 1 h and 16 h, and DNA band changes were compared by agarose gel electrophoresis. The results showed that there was no non-specific nuclease residue in BsaI.

Figure2. The end integrity is good and the effect is consistent with imported brands
When BsaI and substrate DNA were incubated in the enzyme digestion reaction system for 16 hours at 37°C, no non-specific degradation of the substrate caused by star activity was detected, indicating that there was no star activity after 16 hours of incubation with BsaI.
Documents
Citations
Safety Data Sheet
10661_MSDS_HB240611_EN.PDF
Download
Manuals
10661_Manual_HB20241220_EN.PDF
Download
Payment & Security
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