FAQs | AmbioPharm

FAQs

Find answers to some common peptide Frequently Asked Questions (FAQs) below or contact us.

Can you synthesize peptides with post-translational modifications?

Do you make peptides as a starting material for radiolabeled peptides?

What synthesis approach should be taken for a toxicology (tox) and Phase I batch?

When do I need cGMP peptides?

Do you have any useful tools for the peptide researcher?

Which salt form should I choose for my peptide?

What does cGMP mean?

Why should you consider pegylated peptides?

Do you manufacture peptides with disulfide bonds or other cyclization motifs?

What is the advantage of capping the N and C termini of the peptide?

What quality control data do you provide for non-GMP grade peptides?

How do you introduce the dye when making fluorescently-labeled peptides?

What purity percentage is required?

Do you provide cGMP-grade peptides?

How are peptides synthesized?

What is the maximum peptide length you can synthesize?

What causes delays in peptide delivery?

What methods do you use to synthesize peptides?

What is a counterion?

What is the best way to dissolve peptides?

How should you store peptides?

How is theoretical net peptide content calculated?

What is net peptide content?

What peptide purification methods do you use?

What is the typical purity percentage of custom peptides?

What data is provided on the Certificate of Analysis (CoA)?

How do you place an order for peptide services?

What is the typical lead time for non-GMP custom peptide synthesis at AmbioPharm?

Counterfeit Products

Do you use consultants or distributors to sell your products?

Do you sell generic peptides?

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