Anti-SorLA/SORL1 antibody [EPR23262-4] (BSA and Azide free)
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal SorLA/SORL1 antibody. Carrier free. Suitable for ICC/IF, IHC-Fr and reacts with Mouse, Human, Rat samples.
View Alternative Names
C11orf32, SORL1, Sortilin-related receptor, Low-density lipoprotein receptor relative with 11 ligand-binding repeats, SorLA-1, Sorting protein-related receptor containing LDLR class A repeats, LDLR relative with 11 ligand-binding repeats, LR11, SorLA
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SorLA/SORL1 antibody [EPR23262-4] (BSA and Azide free) (AB302509)
This data was developed using ab302508, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized SK-BR-3 (human breast adenocarcinoma epithelial cell) cells labelling SorLA/SORL1 with ab302508 at 1/50 (10.32 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2ug/mL dilution (Green). Confocal image showing cytoplasmic staining in SK-BR-3 cell lineNegative control : MDA-MB-231 (PMID : 31138794) is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2ug/mL dilution.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-SorLA/SORL1 antibody [EPR23262-4] (BSA and Azide free) (AB302509)
This data was developed using ab302508, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat cerebrum (fresh) tissue labeling SorLA/SORL1 with ab302508 at 1/500 (1.032 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Positive staining on rat cerebrum is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution. .
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SorLA/SORL1 antibody [EPR23262-4] (BSA and Azide free) (AB302509)
This data was developed using ab302508, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized mouse primary neural/glia cells labeling SorLA/SORL1 with ab302508 at 1/50 dilution (10.32 µ/mL), followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preabsorbed antibody at 1/1000 dilution (2µ/mL) (Green). Confocal image showing cytoplasmic staining in mouse primary neural/glia cell. Confocal scanning Z step was set as 0.3 μm followed by image processing with maximum Z projection. Negative control : NIH/3T3 (PMID : 11082041) . ab11267 Anti-MAP2 mouse monoclonal antibody was used to counterstain tubulin at 1/500 4µ/mL dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody control : Primary diluent was used instead of primary antibody, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preabsorbed at 1/1000 dilution (2µ/mL).
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-SorLA/SORL1 antibody [EPR23262-4] (BSA and Azide free) (AB302509)
This data was developed using ab302508, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse cerebrum (fresh) tissue labeling SorLA/SORL1 with ab302508 at 1/500 (1.032 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Positive staining on mouse cerebrum is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution. .
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-SorLA/SORL1 antibody [EPR23262-4] (BSA and Azide free) (AB302509)
This data was developed using ab302508, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat lung (fresh) tissue labeling SorLA/SORL1 with ab302508 at 1/500 (1.032 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Negative control : no staining on rat lung (PMID : 9157966) is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution. .
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-SorLA/SORL1 antibody [EPR23262-4] (BSA and Azide free) (AB302509)
This data was developed using ab302508, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse skeletal muscle (fresh) tissue labeling SorLA/SORL1 with ab302508 at 1/500 (1.032 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Negative control : no staining on mouse skeletal muscle (PMID : 9157966) is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution. .
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-SorLA/SORL1 antibody [EPR23262-4] (BSA and Azide free) (AB302509)
This data was developed using ab302508, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat skeletal muscle (fresh) tissue labeling SorLA/SORL1 with ab302508 at 1/500 (1.032 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Negative control : no staining on rat skeletal muscle (PMID : 9157966) is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution. .
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-SorLA/SORL1 antibody [EPR23262-4] (BSA and Azide free) (AB302509)
This data was developed using ab302508, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse lung (fresh) tissue labeling SorLA/SORL1 with ab302508 at 1/500 (1.032 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Negative control : no staining on mouse lung (PMID : 9157966) is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution. .
Related conjugates and formulations (1)
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Anti-SorLA/SORL1 antibody [EPR23262-4]
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Biological function summary
SorLA acts as a sorting receptor and contributes significantly to the regulation of protein sorting and signaling pathways within the cell. SorLA interacts with various ligands and forms complexes including lipid transport proteins and neuropeptides. The protein also plays a role in the sorting of the amyloid precursor protein (APP) assisting in the regulation of its processing and reducing the production of amyloid-beta a component significant in neurodegenerative processes.
Pathways
SorLA participates actively in the cellular pathways associated with protein trafficking and processing. It is integral to pathways involving endocytosis and the regulation of APP processing. SorLA interacts with important proteins such as APP and the low-density lipoprotein receptor-related protein 1 (LRP1). These interactions exemplify SorLA’s critical involvement in the cellular maintenance of protein homeostasis and in mitigating the production of potentially pathogenic peptides therefore interfacing with wider neurobiological functions.
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