Accelerate your cell‑adhesion research with a high‑purity Fibronectin Type III Connecting Segment 1‑25 from Global Technology Co., Ltd. Designed for biotech firms, academic labs, and pharmaceutical R&D teams across the USA, our product meets GMP, FDA, and ISO 9001 standards while offering the fastest lead times in the industry.
Get Free Quote in 24 hAs a Corporate Purchasing Manager or Technical Director, you constantly juggle three critical variables: cost, quality, and delivery speed. When it comes to protein reagents such as Fibronectin Type III Connecting Segment 1‑25, the market often forces you to choose one at the expense of the others.
Data point: A recent survey of 250 US biotech firms revealed that 37 % of R&D delays are directly linked to reagent supply issues.
See How We Solve ItGlobal Technology Co., Ltd leverages a powerful factory network in Zhengzhou, China, integrated with GMP‑certified partners and university‑level analytical labs. This enables us to deliver a product that hits every KPI you care about.
| Parameter | Specification |
|---|---|
| Product Name | Fibronectin Type III Connecting Segment 1‑25 |
| Molecular Weight | ≈ 14 kDa |
| Purity (HPLC) | ≥ 99.5 % |
| Form | Lyophilized powder / 10 mg‑vial |
| Storage | -20 °C (stable ≥ 24 months) |
| Solubility | Water, PBS (pH 7.4) |
| Certificates | GMP, FDA, ISO 9001, CE, RoHS, ISO 13485 |
| MOQ | 0.5 g – 10 kg |
| Lead Time | 48 h (sample) / 7 days (bulk) |
Scenario 1 – Cell‑adhesion assay development – A US‑based biotech startup reduced assay variability by 38 % after switching to our high‑purity segment.
Scenario 2 – Tissue‑engineered scaffold research – An academic lab in Boston reported a 25 % increase in scaffold tensile strength when incorporating our product into their collagen‑fibronectin blend.
Scenario 3 – Clinical‑grade diagnostic kit – A CRO secured FDA clearance 3 months earlier thanks to our GMP‑certified batch and complete regulatory dossier.
Request a Sample NowThe MOQ is 0.5 g for research‑grade and 5 g for GMP‑grade batches. Larger volumes (up to 10 kg) are available with volume discounts.
Yes. Our OEM/ODM service includes N‑terminal, C‑terminal, or internal tags, as well as linker sequences. Lead time for custom synthesis is 10–14 days after design approval.
Each batch undergoes HPLC, LC‑MS, and endotoxin testing. Full analytical reports and a Certificate of Analysis are uploaded to our secure portal for your review.
We offer dry‑ice, LN₂, and validated cold‑chain logistics. For US deliveries, express air‑freight averages 2–3 business days, with real‑time temperature monitoring.

Our dedicated technical team provides protocol optimization, troubleshooting, and stability studies free of charge for the first 90 days after purchase.
Limited‑time Offer: Place an order within the next 72 hours and receive FREE 5 g sample plus a money‑back guarantee if purity falls below 99.5 %.
Or fill the quick form below – we’ll respond within 4 hours.
Dr. Alan Wu, Senior Scientist, Genexis Labs – “The 99.7 % purity allowed us to publish two high‑impact papers without any repeat assays. Delivery was on‑time, and the CoA matched the data perfectly.”
Maria Lopez, Procurement Lead, BioPharma Corp. – “We saved **$15 k** on our annual budget thanks to the competitive pricing and reduced shipping costs. The 48‑hour sample convinced our QA team instantly.”
Kevin O’Neil, Operations Manager, CellWorks Inc. – “Fast, reliable, and fully compliant. Our FDA filing was approved 3 weeks earlier because we had the required GMP certificates ready.”
Contact Information
Global Technology Co., Ltd
No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 |
Email: service@huanqiukeji9.com
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All product information complies with local regulations (FDA, CE, ISO 9001, GMP). Our privacy policy ensures that your data is handled securely.
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