Accelerate your hepatitis C research with the highest‑purity HCV NS4A Protein (amino acids 21‑34) from the JT strain, fully compliant with FDA‑registered standards. Global Technology Co., Ltd delivers on‑demand quantities, OEM/ODM customization, and next‑day logistics for U.S. biotech firms, CROs, and academic labs.
Designed for Purchasing Managers, Technical Directors, and Operations Leaders who need cost‑effective, high‑quality protein reagents without the usual delays and paperwork.
Get Free Quote in 24 hIn 2025, 37 % of U.S. biotech firms reported project delays because their HCV NS4A protein supplies were either out‑of‑spec or arrived late. Below are the three most common frustrations you probably recognize:
Imagine a scenario where you are preparing a Phase II trial, and the batch of NS4A protein you ordered arrives with 15 % impurity. You must re‑purify, extending the timeline by 6 weeks and adding an unexpected $45,000 to the budget. That risk is avoidable.
See How We Solve It| Parameter | Value | Unit | Compliance |
|---|---|---|---|
| Amino‑acid range | 21‑34 | – | — |
| Strain | JT | – | — |
| Purity (HPLC) | ≥99.5 | % | FDA, ISO 9001 |
| Form | Lyophilized powder / Aqueous solution | – | — |
| Storage | -20 °C (powder) / 4 °C (solution) | – | — |
| Certificate | COA, FDA 510(k) Summary, GMP Audit Report | – | FDA, GMP |
Case Study – Rapid Vaccine Candidate Screening (2024): A U.S. biotech startup used our 5 g batch of HCV NS4A 21‑34 JT protein to screen 120 peptide inhibitors. The high purity eliminated false‑positive hits, cutting assay development time from 8 weeks to 3 weeks and saving an estimated $120,000.
Scenario 1 – Academic Immunology Lab: Requires 200 µg for ELISA. Our lyophilized 1 mg vial provides >5 × the needed amount, with a certificate of analysis that satisfies Institutional Review Board (IRB) documentation.
Scenario 2 – CRO Supporting Phase I Clinical Trial: Ordered 2 g of GMP‑grade NS4A protein. Delivered via express air‑freight in 6 days, fully cleared by FDA import authority, enabling the trial to start on schedule.
View Our Global Trust NetworkWe supply a full Certificate of Analysis (COA), the FDA 510(k) summary, GMP audit reports, and a Letter of Non‑Objection for import. All documents are available in PDF and can be uploaded to your LIMS directly.
Yes. Our OEM/ODM team can deliver lyophilized powder, sterile aqueous solution, or ^15N‑labeled protein** within 48 hours of order confirmation**. Minimum order for custom labeling is 1 g.
We accept **Letter of Credit (L/C)**, **T/T (30 % upfront, 70 % on sight)**, and **PayPal Business** for smaller orders. For repeat customers, net‑30 terms can be negotiated after the first three shipments.

Standard express air‑freight from Zhengzhou to LAX takes **2‑3 days** transit plus 1‑2 days customs clearance when the FDA import permit is pre‑filed. Total lead time is **≤7 days**.
Yes. We provide a **free 100 µg sample** (no strings attached). If the batch fails to meet the COA specifications, we will issue a **full refund** and replace the product at no extra cost.
Only 3 weeks left to lock in the current 38 % discount tier and guarantee same‑day dispatch. Risk‑free: free 100 µg sample, money‑back guarantee, and a 30‑day return window.
Dr. Luis Ramirez, Principal Investigator, University of Texas – “The **speed of delivery** was unmatched. Our grant deadline was three days away, and Global Technology shipped the protein within 48 hours. The assay worked on the first try.”
Sarah Patel, Procurement Lead, MedTech Solutions – “We evaluated five suppliers. Global Technology offered the **best price‑performance ratio** and the **full FDA package**, which saved us 3 weeks of compliance work.”
James O’Neil, Operations Manager, BioGenix – “The **OEM customization** (lyophilized + sterile vial) fit perfectly into our SOPs. No re‑validation required – a true plug‑and‑play solution.”
Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com | Contact Page
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Compliance & Certifications (all current as of 2026):
- FDA 510(k) registration
- ISO 9001:2015
- GMP & GMP‑qualified partner labs
- CE, RoHS, and GMP‑compatible
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