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Polyethylene glycol (PEG) antibodies

abinScience offers high-specificity monoclonal and polyclonal antibodies targeting PEG backbone (anti-PEG) and methoxy terminus (anti-mPEG) for ADA (anti-drug antibody) screening, confirmatory, titer, and PK ELISA applications. Conjugation options include HRP, Biotin, and fluorescent labels (AF488/AF647). Each lot includes a Certificate of Analysis (CoA) with purity, endotoxin, and performance data. RUO

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Selection guide

  1. Epitope: Select anti-PEG for broad backbone recognition; use anti-mPEG for terminal-specific binding or compatibility with mPEG-coated systems; choose anti-PEGylated-protein for drug-specific applications.
  2. Clonality/Isotype: IgM provides high avidity and multivalent binding—ideal for capture or screening; IgG is preferred for detection, confirmatory steps, and competitive formats. Pair according to bridge or direct assay design.
  3. Conjugate: HRP or Biotin for standard PK/ADA ELISA; AF488/AF647 for flow cytometry or immunofluorescence; unconjugated or HRP for Western blot.
  4. Matrix: Refer to CoA for minimum required dilution (MRD) and spiked recovery data. Avoid interference from polysorbates or surfactants.
  5. Assay design: Follow ADA workflow: Screening → Confirmatory (drug competition) → Titer. Apply 4PL/5PL curve fitting with negative/positive controls and low/medium/high QC samples.

Applications

Spotlight

 

Anti-PEG (backbone), IgM-HRP

High avidity • Screening/PK capture • Lot-specific CoA

 

Anti-mPEG (terminal), IgG-Biotin

Confirmatory compatible • Bridge/competitive • Low background

 

Anti-PEGylated-protein, IgG

Drug-specific • PK/ADA workflows • Matched controls available

FAQs

What is the difference between anti-PEG and anti-mPEG?

anti-PEG recognizes the repeating backbone unit (—CH₂CH₂O—) and offers broad applicability across PEG sizes. anti-mPEG preferentially binds the methoxy terminal group and is optimized for use with mPEG-BSA coated plates or terminal-specific analysis.

How to choose between IgG and IgM?

IgM delivers high-avidity, multivalent binding—ideal for capture antibodies in screening or PK assays. IgG is better suited for detection, confirmatory steps, and competitive inhibition assays. Selection depends on assay readout (A₄₅₀, titer, % inhibition) and background signal.

Are there matrix or surfactant interferences?

Formulations containing polysorbate (Tween) or other surfactants may interfere with binding or increase background. Always follow the CoA-recommended MRD, validate spiked recovery, and include blank matrix controls.

RUO disclaimer

All products are for Research Use Only (RUO) and are not intended for diagnostic or therapeutic procedures.

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