PTH Antibody Pair

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Description

Definition and Purpose

PTH Antibody Pair refers to a matched set of two antibodies designed for the quantitative detection of human parathyroid hormone (PTH) in immunoassays. These pairs typically include a capture antibody (e.g., monoclonal) and a detection antibody (e.g., polyclonal or enzyme-conjugated), enabling precise measurement of intact PTH or specific fragments in biological samples .

Antibody Pair Composition

ComponentHost SpeciesTarget RegionFormatExample Products
Capture AntibodyMouseC-terminalMonoclonal (IgG1κ)Abnova H00005741-AP51
Detection AntibodyRabbitN-terminalPolyclonal (HRP-conj)Novus NBP2-79411

Mechanism:

  • Sandwich ELISA/IRMA: The capture antibody immobilizes PTH via its C-terminal region, while the detection antibody binds the N-terminal epitope, enabling signal amplification (e.g., chemiluminescence or radioactivity) .

  • Specificity: Designed to minimize cross-reactivity with inactive PTH fragments (e.g., C-terminal fragments common in renal failure) .

Applications in Clinical and Research Settings

  1. Renal Disease Management:

    • Detects intact PTH (1–84) in patients with chronic kidney disease, critical for diagnosing secondary hyperparathyroidism .

    • Third-generation assays differentiate oxidized PTH (biologically inactive) using anti-oxidized PTH monoclonal antibodies .

  2. Cancer Research:

    • Ultrasensitive microfluidic assays (limit: 0.3 fg/mL) for PTH-related peptides (PTHrP) aid in diagnosing aggressive prostate and breast cancers .

  3. Bone Metabolism Studies:

    • Evaluates thymus-derived PTH in murine models post-thyroparathyroidectomy, revealing compensatory hormone production .

Comparative Assay Performance

Assay TypeSensitivityDynamic RangeCross-ReactivityReference
Magnetic Particle IRMA8–12 μCi/μg0–2,000 pg/mLHuman-specific
Polystyrene Tube ELISA312.5 pg/mL312.5–20,000 pg/mLHuman-specific
Microfluidic Immunoarray0.3 fg/mL0.3–10,000 fg/mLPTHrP isoforms

Critical Observations:

  • Antibody Compatibility: Polyclonal C-terminal antibodies paired with DiaSorin tracers showed optimal binding in IRMA development .

  • Oxidation Interference: Methionine oxidation at residues 8/18 reduces PTH bioactivity, necessitating specialized columns for oxidized PTH removal .

Challenges and Innovations

  1. Fragment Interference: Early assays detected inactive C-terminal fragments, but second-generation IRMA improved specificity using dual-epitope targeting .

  2. Tracer Degradation: Radioiodinated tracers lose sensitivity within a month, necessitating frequent recalibration .

  3. Species Cross-Reactivity: PTH1R antibodies (e.g., Proteintech 29115-1-AP) enable cross-species receptor studies in human, mouse, and rat models .

Future Directions

  • Multiplex Assays: Integrating PTHrP with biomarkers like VEGF-D enhances diagnostic accuracy for aggressive cancers .

  • Non-Radioactive Labels: Transitioning to chemiluminescent or electrochemical detection improves safety and scalability .

Product Specs

Buffer
**Capture Buffer:** 50% Glycerol, 0.01M PBS, pH 7.4
**Detection Buffer:** 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
Typically, we can ship your order within 1-3 business days of receipt. Delivery timelines may vary based on your chosen shipping method and location. Please contact your local distributor for specific delivery estimates.
Notes
For optimal results, we recommend using the capture antibody at a concentration of 0.5 µg/mL and the detection antibody at a concentration of 0.2 µg/mL. We encourage researchers to determine the optimal dilutions experimentally.
Synonyms
Parathormone,Parathyrin,PTH

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