Mouse monoclonal antibody to human SORL1 (SorLA) [3B6B11]

Antibodies

貨號 Cat. No.
M-1934-100
規格 Size
100 µL
品牌 Brand
Biosensis
Application 應用
IC 、 IF 、 IH(P) 、 WB
Reactivity
Human
Host
Mouse
Clonality
Monoclonal
Conjugate
IgG1

Description




ZZZZ_Status (Active, Disc) : Active


 

AA_Supplier Name : Biosensis


 

Alternative_Name (Other Names) :


Sortilin-related receptor; Low-density lipoprotein receptor relative with 11 ligand-binding repeats; LDLR relative with 11 ligand-binding repeats; LR11; SorLA-11; Sorting protein-related receptor containing LDLR class A repeats; SorLA


 

Antibody_Isotype
(Antibody only) :


 

Application_Details :


Western Blotting (1:500-1:2,000), Immunohistochemistry (1:200-1:1,000, use at 1:200 for paraffin-embedded tissues), Immunocytochemistry (1:200-1:1,000) and ELISA (1:10,000). Other applications have not been tested. Biosensis recommends optimal dilutions/concentrations should be determined by the end user.


 

Background_Info :


 

Clone_Name
(AB only, monoclonals) : 3B6B11


 

Datasheet_Link : https://www.biosensis.com/pdf_datasheet.php?products_id=1835


 

Description (Long Description) : 


The sortilin-related receptor SORLA is an endocytic receptor that belongs to the vacuolar protein sorting 10 (VPS10) domain receptor family. SORLA binds to the amyloid precursor protein (APP). It functions as an intracellular sorting receptor as APP is being trafficked between the secretory pathway, the cell surface, and, subsequently, endosomes. SORLA is localized primarily to the trans-Golgi network and early endosomes, shuttling between these two membrane compartments. SORLA’s interaction with APP in endosomal compartments limits the amyloidogenic proteolysis of APP. Reduced brain levels of SORLA are thought to alter the transport and processing of APP to increase generation of Aβ peptides in early or late endosomes. SORLA is highly expressed in the brain. Expression is reported to be normal in familial Alzheimer's disease caused by mutations in presenilin or APP genes, but decreased in some cases of sporadic late-onset AD. In these cases, loss of SORLA activity has been hypothesized to be a proximal cause of amyloidosis. In addition, several private nonsense and missense mutations in SORLA that decrease SORLA levels in the brain were found in rare cases of familial AD. A genetic association of SORLA with AD is well established. Population-based studies initially linked nearly 30 SNPs in SORLA to increased risk of AD, and subsequent studies, meta-analyses, and GWAS have confirmed some of these associations. The genetic data on SORLA and LOAD is complex, with at least six different polymorphisms pointing toward the existence of several causative variants in distinct regions of the gene. Ref: alzforum.org

 

Expiry_Date : 


12 months after purchase if unopened and stored at -20C.

 

Format (Form) : 


Ascitic fluid containing 0.03% sodium azide

 

Immunogen (Antigen) :Purified recombinant fragment of human SorLA expressed in E. Coli


 

Kit_Components :


 

MSDS (File name) :


 



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