Date published: 2026-5-13

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LRP1 Antibody (5A6): sc-57351

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Datasheets
  • LRP1 Antibody (5A6) is a mouse monoclonal IgG2b LRP1 antibody, cited in 12 publications, provided at 100 µg/ml
  • raised against full length native LRP1 of human origin
  • recommended for detection of 85 kDa cleaved fragment of Low Density LRP1 of mouse, rat and human origin by WB (non-reducing), IF, IHC(P) and FCM
  • m-IgG Fc BP-HRP and m-IgG2b BP-HRP are the preferred secondary detection reagents for LRP1 Antibody (5A6) for IHC(P) applications. These reagents are now offered in bundles with LRP1 Antibody (5A6) (see ordering information below).
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LRP1 Antibody (5A6) is a mouse monoclonal IgG2b antibody designed to detect Low-Density Lipoprotein Receptor-Related Protein 1 (LRP1), also known as α2-Macroglobulin Receptor (α2MR). LRP1 is a large, multifunctional endocytic receptor characterized by its complex structure, which includes clusters of cysteine-rich class A repeats, epidermal growth factor (EGF)-like repeats, YWTD repeats, and an O-linked sugar domain. This intricate architecture enables LRP1 to interact with a diverse array of ligands, facilitating essential processes such as lipid metabolism, protease clearance, and cellular signaling. The structural integrity of LRP1 is crucial for maintaining cellular homeostasis and enabling the uptake of over fifteen different ligands, including α2-Macroglobulin and apolipoprotein E (apoE). LRP1 is predominantly expressed on the cell surface in key tissues like the brain, liver, and lungs, highlighting its importance in neurological health, metabolic regulation, and respiratory function. Anti-LRP1 antibody (5A6) targets the full-length native human LRP1, specifically recognizing the 85 kDa cleaved fragment of the protein across multiple species, including mouse, rat, and human for applications such as western blotting (WB), immunofluorescence (IF), immunohistochemistry (IHC), and flow cytometry (FCM). By enabling precise analysis of LRP1′s structural domains, LRP1 (5A6) antibody supports advanced studies into its critical roles in physiological processes and involvement in pathological conditions like Alzheimer′s disease, where the LRP1 gene is located at a significant locus on chromosome 12.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

LRP1 Antibody (5A6)

sc-57351
100 µg/ml
$322.00

LRP1 Antibody (5A6): m-IgG Fc BP-HRP Bundle

sc-539054
100 µg Ab; 10 µg BP
$361.00

LRP1 Antibody (5A6): m-IgG2b BP-HRP Bundle

sc-549729
100 µg Ab; 10 µg BP
$361.00

I did IHC on paraffin section of mouse brain and used mouse liver as a positive control a few days ago.I found no signal even on positive control. I did antigen retrival with EDTA and used a dilution of 1:50, incubated in 4 celcieus overnight.

Asked by: eugene02
Thank you for your question. Please reach out to our technical service team so they can offer troubleshooting advice on your experiment.
Answered by: Technical Support Europe
Date published: 2020-10-23

What is the recommended secondary reagent to be used with this mouse monoclonal primary?

Asked by: jerojero
We recommend using one our exclusive Mouse IgG Binding Proteins as a secondary detection reagent. A complete list of available binding proteins is available on our website here: https://www.scbt.com/scbt/browse/support-products-mouse-igg-binding-proteins/_/N-ecrety
Answered by: Technical Support 8
Date published: 2017-01-09
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Rated 4 out of 5 by from Tested on HFFF by FACSThis antibody was tested on HFFF cells by FACS and gave a satisfactory signal at dilution 1:25
Date published: 2018-11-16
Rated 5 out of 5 by from Reliable Antibody, Great for FlowThis antibody is well-cited for a variety of applications including IP, IF, and even Flow Cytometry. Reliable antibody.
Date published: 2017-01-16
Rated 5 out of 5 by from Superb indirect FCM analysis of Hep G2 cellsSuperb indirect FCM analysis of Hep G2 cells stained with LRP1 . -SCBT QC
Date published: 2014-02-15
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LRP1 Antibody (5A6) is rated 4.7 out of 5 by 3.
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