SorLA Antibodies
We offer SorLA Antibodies for use in common research applications: ELISA, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Immunohistochemistry-Frozen, Immunohistochemistry-Paraffin, Peptide ELISA, Sandwich ELISA, Western Blot. Each SorLA Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our SorLA Antibodies can be used in a variety of model species: Human, Mouse. Use the list below to choose the SorLA Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our SorLA polyclonal antibodies and browse our SorLA monoclonal antibody catalog.
Alternate Names for SorLA Antibodies
anti-SorLA antibody, anti-SORL1 antibody, anti-C11orf32 antibody, anti-chromosome 11 open reading frame 32 antibody, anti-FLJ21930 antibody, anti-FLJ39258 antibody, anti-gp250 antibody, anti-Low-density lipoprotein receptor relative with 11 ligand-binding repeats antibody, anti-LR11LDLR relative with 11 ligand-binding repeats antibody, anti-LRP9 antibody, anti-mosaic protein LR11 antibody, anti-SorLA-1SORLA antibody, anti-sortilin-related receptor antibody, anti-sortilin-related receptor, L(DLR class) A repeats containing antibody, anti-sortilin-related receptor, L(DLR class) A repeats-containing antibody, anti-Sorting protein-related receptor containing LDLR class A repeats antibody
8 Results for "sorla" in Primary Antibodies
![Immunofluorescence: SorLA Antibody [NB100-785] - Analysis of paraformaldehyde fixed A431 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing cytoplasmic with endosome staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](http://images.novusbio.com/fullsize/SorLA-Antibody-Immunofluorescence-NB100-785-img0001.jpg "Immunofluorescence: SorLA Antibody [NB100-785] - Analysis of paraformaldehyde fixed A431 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing cytoplasmic with endosome staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).")
![Immunofluorescence: SorLA Antibody [NB100-785] - Analysis of paraformaldehyde fixed HepG2 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing cytoplasmic/endosome, membrane and nuclear staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](http://images.novusbio.com/fullsize/SorLA-Antibody-Immunofluorescence-NB100-785-img0002.jpg)
![Western Blot: SorLA Antibody (3B6B11) [NBP1-28882] - Analysis using SORL1 mouse mAb against truncated SORL1 recombinant protein.](http://images.novusbio.com/fullsize/SorLA-Antibody-3B6B11-Western-Blot-NBP1-28882-img0011.jpg "Western Blot: SorLA Antibody (3B6B11) [NBP1-28882] - Analysis using SORL1 mouse mAb against truncated SORL1 recombinant protein.")
![Immunocytochemistry/Immunofluorescence: SorLA Antibody (3B6B11) [NBP1-28882] - Analysis of PANC-1 cells using SORL1 mouse mAb (green). Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin. Blue: DRAQ5 fluorescent DNA dye.](http://images.novusbio.com/fullsize/SorLA-Antibody-3B6B11-Immunocytochemistry-Immunofluorescence-NBP1-28882-img0008.jpg)
![Immunohistochemistry-Paraffin: SorLA Antibody (3B6B11) [NBP1-28882] - Analysis of human cerebrum tissues using SORL1 mouse mAb with DAB staining.](http://images.novusbio.com/fullsize/SorLA-Antibody-3B6B11-Immunohistochemistry-Paraffin-NBP1-28882-img0010.jpg)
![Immunohistochemistry-Paraffin: SorLA Antibody (3B6B11) [NBP1-28882] - Analysis of human brain, cortex tissues using SORL1 mouse mAb.](http://images.novusbio.com/fullsize/SorLA-Antibody-3B6B11-Immunohistochemistry-Paraffin-NBP1-28882-img0009.jpg)
![Western Blot: SorLA Antibody (JE35-52) [NBP3-32967] - Western blot analysis of SorLA on Jurkat cell lysates with Rabbit anti-SorLA antibody (NBP3-32967) at 1/1,000 dilution. Lysates/proteins at 20 ug/Lane. Predicted band size: 248 kDa Observed band size: 248 kDa Exposure time: 1 minute 30 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32967) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32967_rabbit-sorla-mab-je35-52-288202412493426.jpg "Western Blot: SorLA Antibody (JE35-52) [NBP3-32967] - Western blot analysis of SorLA on Jurkat cell lysates with Rabbit anti-SorLA antibody (NBP3-32967) at 1/1,000 dilution. Lysates/proteins at 20 ug/Lane. Predicted band size: 248 kDa Observed band size: 248 kDa Exposure time: 1 minute 30 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32967) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: SorLA Antibody (JE35-52) [NBP3-32967] - Immunohistochemical analysis of paraffin-embedded mouse cerebellum tissue with Rabbit anti-SorLA antibody (NBP3-32967) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32967) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32967_rabbit-sorla-mab-je35-52-298202414262695.jpg)
![Western Blot: SorLA Antibody (SR1433) [NBP3-22079] - Western blot analysis using NBP3-22079 in SH-SY5Y cell lysate.](http://images.novusbio.com/fullsize/nbp3-22079_rabbit-sorla-mab-sr1433-5720231552183.jpg "Western Blot: SorLA Antibody (SR1433) [NBP3-22079] - Western blot analysis using NBP3-22079 in SH-SY5Y cell lysate.")
![Immunohistochemistry: SorLA Antibody [NBP2-38177] - Staining of human cerebellum shows strong cytoplasmic positivity in Purkinje cells.](http://images.novusbio.com/fullsize/SorLA-Antibody-Immunohistochemistry-NBP2-38177-img0002.jpg "Immunohistochemistry: SorLA Antibody [NBP2-38177] - Staining of human cerebellum shows strong cytoplasmic positivity in Purkinje cells.")
![ELISA: SorLA Antibody (3F2) [H00006653-M01] - Detection limit for recombinant GST tagged SORL1 is approximately 3ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/SorLA-Antibody-3F2-Sandwich-ELISA-H00006653-M01-img0002.jpg "ELISA: SorLA Antibody (3F2) [H00006653-M01] - Detection limit for recombinant GST tagged SORL1 is approximately 3ng/ml as a capture antibody.")