Procollagen Type I N-Terminal Propeptide (PINP) Antibody (Biotin)

Este producto es parte de PINP-Procollagen Type I N-Terminal Propeptide
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403€ (200 µl)

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935106861
info@markelab.com
name
Procollagen Type I N-Terminal Propeptide (PINP) Antibody (Biotin)
category
Primary Antibodies
provider
Abbexa
reference
abx273392
tested applications
WB, IHC, IF/ICC

Description

Procollagen I N-Terminal Propeptide (PINP) Antibody (Biotin) is a Rabbit Polyclonal antibody conjugated to Biotin against Procollagen I N-Terminal Propeptide (PINP).

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Procollagen Type I N-Terminal Propeptide (PINP)
Host
Rabbit
Reactivity
Rat
Recommended Dilution
WB: 0.5-2 µg/ml, IHC: 5-20 µg/ml, IF/ICC: 5-20 µg/ml. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Biotin
Isotype
IgG
Purification
Purified by antigen-specific affinity chromatography.
Size 1
200 µl
Size 2
1 ml
Form
Liquid
Tested Applications
WB, IHC, IF/ICC
Buffer
0.01 M PBS, pH 7.4, containing 0.05% Proclin-300, 50% glycerol.
Availability
Shipped within 5-15 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
Alias
PINP,P1NP
Background
Antibody anti-PINP
Status
RUO

Descripción

Procollagen Type I N-Terminal Propeptide (PINP) is a cleavage product released during the biosynthesis of type I collagen, which is the most abundant collagen type found in bones, skin, and connective tissues. It serves as a sensitive and specific biomarker for bone formation, reflecting the activity of osteoblasts and the overall rate of collagen synthesis. PINP is widely used in clinical and research settings to monitor bone metabolism, particularly in conditions such as osteoporosis, Paget's disease, and metabolic bone disorders. It is often measured to assess the effectiveness of anabolic or anti-resorptive treatments in improving bone health. PINP levels can also indicate increased collagen turnover in fibrotic diseases, including liver fibrosis and systemic sclerosis, where excessive extracellular matrix production occurs. PINP exists in two forms in circulation, the intact trimer and a smaller monomer, both of which are measurable through immunoassays. The protein's dynamic association with bone remodeling and extracellular matrix synthesis underscores its importance as a marker for tissue repair and fibrotic activity. Emerging research highlights its potential in oncology, where altered PINP levels are linked to metastatic bone disease and tumor-induced bone resorption.

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