Rapid, high‑purity HBsAg epitope peptide engineered for ELISA, rapid test strips, and next‑generation immunoassays. Global Technology Co., Ltd delivers OEM/ODM design, GMP‑certified quality, and high‑speed delivery to U.S. diagnostics manufacturers.
Get Your Free Sample in 48 h1. Sky‑rocketing peptide costs – Most suppliers quote > $500 / mg for HBsAg epitope peptide, eroding profit margins.
2. Inconsistent purity & activity – Batch‑to‑batch variation of > 5 % leads to failed validation runs and costly re‑work.
3. Slow lead times – Conventional manufacturers require 6‑8 weeks, delaying product launches and market share capture.
4. Complex regulatory compliance – Lack of CE, FDA, ISO‑9001 documentation forces extra internal QA effort.
5. Expensive freight & customs – Shipping from distant Asian hubs adds 30‑40 % to total landed cost.
According to a 2025 industry survey, 37 % of diagnostic firms cite peptide supply bottlenecks as the top barrier to scaling rapid‑test production. If you’re still wrestling with these issues, you’re losing both time and revenue.
| Parameter | Value | Unit | Compliance |
|---|---|---|---|
| Sequence | “…” (customizable) | ‑ | N/A |
| Purity (HPLC) | ≥ 98.5 | % | USP 1 |
| Molecular Weight | ~ 2 kDa (depends on length) | Da | MS‑Verified |
| Solubility | ≥ 10 mg/mL in water | mg/mL | ISO 10993‑5 |
| Stability | 24 months at –20 °C | Months | ICH‑Q1A(R2) |
| Packaging | Cryovial, bulk, or pre‑filled plates | ‑ | ISO 13485 |
ELISA Kit Development – A U.S. biotech firm reduced assay variability from 12 % to 3 % after switching to our peptide, cutting validation time by 40 %.
Rapid Lateral‑Flow Tests – Our lyophilized epitope enabled a 2‑minute visual readout with 95 % sensitivity, allowing the client to file an FDA 510(k) in just 3 months.
Multiplex Immuno‑assays – By supplying custom‑length epitopes (12‑aa vs. 20‑aa), we helped a European CRO expand its panel from 5 to 12 hepatitis‑B markers without re‑optimizing the conjugation chemistry.
Standard synthesis and purification are completed within 5 business days. Expedited (24‑h) service is available for an additional 15 % surcharge.

Yes. Every batch is accompanied by a GMP Certificate of Analysis (CoA), FDA DMF reference, and a full Regulatory Dossier Package (including stability data).
Absolutely. We can synthesize peptides from 8‑30 aa, with N‑/C‑terminal acetylation, biotinylation, or fluorescent tags. Custom orders start at 0.5 g.
We employ a dual‑verification workflow: analytical HPLC (≥ 98 % purity) plus high‑resolution MS. Each batch is cross‑checked against a reference standard stored under controlled conditions.
We ship via DHL Express, UPS, or FedEx with temperature‑controlled packaging. Typical transit time is 2‑4 days, and duties are prepaid for most U.S. customers.
Yes. We provide a free 10 mg sample (no charge, shipping on us) for qualified companies. If the peptide does not meet your specifications, we offer a full refund on the trial order.
Order before 31 May 2026 and receive a 20 % discount on the first 5 g, plus free next‑day shipping to any U.S. address.
Risk‑Free Guarantee: If the peptide fails to meet the CoA specifications, we’ll replace it at no extra cost or issue a full refund.
For any questions, call us at +86 199 4383 0844 or fill out the short form below. Our team responds within 24 hours.
James Liu, Lead Scientist – Horizon Biotech
Laura Martinez, Procurement Director – Apex Health
Dr. Kevin O’Neil, CTO – RapidDiag Inc.
Rachel Kim, Operations Manager – MedLine Solutions
Trusted By Global Leaders & Fully Certified
Certificates & Regulatory Badges
CAS-61043-33-2-GHRH-(1-29)-Amide CAS-321921-71-5-Retatrutide-intermediate C-terminal-fragment-and-modified-histone-substrate CAS-86784-80-7-Sermorelin
What Our Customers Say
“Switching to Global Technology’s HBsAg epitope peptide shaved 3 weeks off our assay development cycle and saved us $85 k in raw‑material costs.”
“The 98.7 % purity met our FDA audit without any additional testing. Delivery in 4 days was a game‑changer for our launch schedule.”
“Custom N‑terminal acetylation was done within 48 h. The regulatory dossier was ready in days, not months.”
Join These Industry Leaders – Get Your Sample