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LDL receptor Recombinant Rabbit mAb (SDT-057-57)

LDL receptor Recombinant Rabbit mAb (SDT-057-57)

Catalog Number: S0B2054 Application: WB,IHC-P Reactivity: Human,Mouse,Rat Conjugation: Unconjugated Brand: Starter
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Regular price $100.00 USD
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Product Details

Product Specification


Host Rabbit
Antigen LDL Receptor
Synonyms Low-density lipoprotein receptor, LDLR
Immunogen Synthetic Peptide
Location Golgi Apparatus, Lysosome, Endosome, Plasma Membrane
Accession P01130
Clone Number SDT-057-57
Antibody Type Rabbit mAb
Application WB, IHC-P
Reactivity Hu, Ms, Rt
Predicted Reactivity Bv, Rb
Purification Protein A
Concentration 0.25mg/ml
Physical Appearance Liquid
Storage Buffer PBS, 40% Glycerol, 0.05%BSA, 0.03% Proclin 300
Stability & Storage

12 months from date of receipt / reconstitution, -20 °C as supplied

Dilution


application dilution species
IHC-P 1:1000
WB 1:500

Background

The low density lipoprotein receptor (LDL R) is the founding member of the LDL R family of scavenger receptors.Binds LDL, the major cholesterol-carrying lipoprotein of plasma, and transports it into cells by endocytosis.LDLR is ubiquitously expressed and is a key receptor for maintaining cholesterol homeostasis in mammals. LDLR-mediated endocytosis is essential for lipoprotein and lipid metabolism.Impaired LDLR function by genetic mutations results in a condition with extremely elevated serum LDL levels and early onset atherosclerosis known as familial hypercholesterolemia (FH).

Picture

Western Blot

WB result of LDL-receptor Rabbit mAb                

Primary antibody: LDL-receptor Rabbit mAb at 1/500 dilution
Lane 1: LNCaP whole cell lysate 20 µg
Lane 2: HEK293 whole cell lysate 20 µg
Lane 3: PC-3 whole cell lysate 20 µg
Lane 4: HepG2 whole cell lysate 20 µg
Lane 5: Hela whole cell lysate 20 µg
Low expression control: HEK293 whole cell lysate    

 low expression control: LNCaP whole cell lysate      

Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 140 kDa
Observed MW: 140 kDa
Exposure time: 120s

WB result of LDL-receptor Rabbit mAb                

Primary antibody: LDL-receptor Rabbit mAb at 1/500 dilution
Lane 1: RAW264.7 whole cell lysate 20 µg
Lane 2: rat liver whole cell lysate 20 µg

Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 140 kDa
Observed MW: 140 kDa
Exposure time: 180s

Immunohistochemistry

IHC shows positive staining in paraffin-embedded human liver.

Anti-LDL receptor antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

Counterstained with hematoxylin.              

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded human liver cancer.

Anti-LDL receptor antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

Counterstained with hematoxylin.              

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded mouse liver.

Anti-LDL receptor antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

Counterstained with hematoxylin.              

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded mouse stomach.

Anti-LDL receptor antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

Counterstained with hematoxylin.              

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded rat liver.

Anti-LDL receptor antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

Counterstained with hematoxylin.              

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

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