Chicken polyclonal antibody to human Heat Shock Protein 27 (HSP27)

Antibodies

貨號 Cat. No.
C-1700-100
規格 Size
100 uL
品牌 Brand
Biosensis
Application 應用
IC 、 WB
Reactivity
Human
Host
Chicken
Clonality
Polyclonal

Description




ZZZZ_Status (Active, Disc) : Active


 

AA_Supplier Name : Biosensis


 

Alternative_Name (Other Names) :



 

Antibody_Isotype
(Antibody only) : IgY


 

Application_Details :


Western Blotting (WB) and Immunocytochemistry (ICC). A dilution of 1:2,000 - 1:5,000 is recommended for WB. A dilution of 1:1,000 - 1:2,000 is recommended for ICC. Biosensis recommends optimal dilutions/concentrations should be determined by the end user.


 

Background_Info :


 

Clone_Name
(AB only, monoclonals) :


 

Datasheet_Link : http://www.biosensis.com/pdf_datasheet.php?products_id=1273


 

Description (Long Description) : 


The heat shock proteins were discovered, as the name suggests, since they are heavily upregulated when cells are stressed by temperatures above the normal physiological range. They are expressed in unstressed cells also and have a normal function as chaperones, helping other proteins to fold correctly, and are required in much greater amounts if the cell or tissue is stressed by heat. The increased levels are generated transcriptionally under the influence of a powerful transcription factor, the heat shock factor 1 (HSF1). The different heat shock proteins were originally named based on their SDS-PAGE mobility, so HSP27 has an apparent molecular weight of 27kDa. It is an abundant protein even under non-stress conditions and frequently shows up as a major spot on 2 dimensional gels of cells or tissues. It is known to associate with a variety of other proteins such as actin, intermediate filament subunits and ubiquitin and is found both in the cytoplasm and the nucleus of cells. HSP27 can become heavily phosphorylated under the influence of multiple protein kinases particularly as a result of activation of the p38/SAPK pathway. Upregulation of this protein is protective against neurodegenerative diseases at least in certain mouse models (1). Point mutations in the HSP27 gene are associated with two neurological diseases, Charcot-Marie-Tooth disease type 2F and distal hereditary motor neuropathy IIB (2). These diseases are associated with axonal loss apparently following defects in the transport of neurofilaments.



 

Expiry_Date : 


12 months after purchase

 

Format (Form) : 


Lyophilized chicken IgY with 5% trehalose and 0.5% sodium azide.

 

Immunogen (Antigen) :Recombinant full length purified HSP27 from E. coli.


 

Kit_Components :


 

MSDS (File name) :


 



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