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5 Common Lab Mistakes When Handling Peptides And How To Avoid

5 Common Lab Mistakes When Handling Peptides And How To Avoid

Dec 6th 2025

5 Common Lab Mistakes When Handling Peptides (And How to Avoid Them)

Updated December 2025 • ~4 min read
Short, practical tips to help technicians and researchers avoid common pitfalls when working with peptides. These are lab-friendly, non-medical best practices you can apply immediately.

Why this matters

Peptides are often delicate and pricey. Small mistakes can reduce yield, alter experimental results, or require re-ordering materials. Below are five mistakes we see frequently and simple steps to prevent them.

1. Shaking Vials After Reconstitution

The mistake: Vigorously shaking peptide vials to dissolve powder quickly.

Why it's a problem: Aggressive shaking can cause foaming, shear forces, or degradation of sensitive peptides, reducing activity or purity.

Fix: Inject solvent slowly against the glass wall and gently swirl the vial until fully dissolved. If a tendon-like pellet remains, let it sit; do not rub or vortex.

2. Using the Wrong Needle or Syringe Size

The mistake: Choosing a large-gauge needle or oversized syringe for small volumes.

Why it's a problem: Thicker needles and larger syringes reduce dosing accuracy, increase solution loss, and may damage vial septa.

Fix: Use a 1 mL or 3 mL syringe for small volumes, and 27G–30G needles for routine reconstitution and transfers. For micro-volumes, consider insulin-style syringes.

3. Not Accounting for Units and Conversions

The mistake: Misreading units (mL vs µL, mg vs µg) or skipping conversion steps.

Why it's a problem: Unit errors can cause 10×–1000× mistakes, wasting material and compromising experiments.

Fix: Always write units clearly, show your math, and use the smallest appropriate device for accuracy (e.g., 1 mL syringe for 0.2 mL). Consider adding an interactive conversion widget to your digital protocols.

4. Reusing Needles or Improper Disposal

The mistake: Reusing needles between vials or failing to dispose of sharps properly.

Why it's a problem: Reuse risks contamination and cross-sample interference. Improper disposal is an occupational safety hazard.

Fix: Use a new sterile needle for each vial or critical transfer. Immediately dispose of used needles in a labeled sharps container. If your protocol requires a capped needle for future use, follow your institutional SOPs.

5. Ignoring Storage and Temperature Recommendations

The mistake: Leaving reconstituted peptides at room temperature or storing lyophilized peptides incorrectly.

Why it's a problem: Many peptides degrade faster at higher temperatures or when exposed to light and moisture.

Fix: Follow the manufacturer's storage instructions: lyophilized peptides are often stored at –20°C or –80°C, while reconstituted solutions may require refrigeration and use within a specified time. Label vials with date/time and initials.

Quick checklist
  • Swab vial tops; use fresh needles.
  • Use 1 mL/3 mL syringes for small volumes.
  • Write units clearly and double-check conversions.
  • Gently swirl — do not shake.
  • Label and store per manufacturer guidance.

Final thoughts

Small changes in technique can improve reproducibility, safety, and cost-efficiency.