Ubiquitin Conjuating Enzyme (E2/UBCE) ELISA Kit (Part hE2UBCE-ELISA)

Ubiquitin Conjuating Enzyme (E2/UBCE) ELISA Kit (Part hE2UBCE-ELISA)
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Price: $635.00
Availability: In Stock
Model: hE2UBCE-ELISA
Manufacturer: Fivephoton Biochemicals

Available Options:
Ubiquitin Conjugating Enzyme E2/UBCE ELISA Kit
 
Ubiquitin Conjugating Enzyme (E2) ELISA Kit
Dynamic Assay Range: 100pg/ml - 30,000pg/ml.  Sensitivity: 37 pg/ml.
 
Lead Time:  Approximately 1.5 weeks
      
View Protocol
 
UBCE ELISA Kit Availability and Specifications
Species
Standard 
Assay Range
 Human 32ng/ml 100pg/ml - 30ng/ml
 Rat 32ng/ml 100pg/ml - 30ng/ml
 Mouse 32ng/ml 100pg/ml - 30ng/ml
 

Highlights
 
 





  • Pre-configured ELISA kit in sandwich assay format.
  • Dynamic Assay Range: 100pg/ml - 30ng/ml.  Sensitivity: 37pg/ml.
  • Standard peptide concentration:  32ng/ml
  • Rapid and simple ELISA Protocol:  Requires one 60 min incubation period at 37oC.
  • Samples are mixed with biotinylated detection antibody and streptavidin-HRP prior to addition to the plate.
  • Available in 96T format.


Intoduction   
to E2/UBCE  
 
 
 
 
 
Ubiquitin-conjugating enzymes are known as E2 enzymes. They perform the second step of ubiquitination. The E2 enzyme receives activated ubiquitin from E1, conjugates it, then binds to E3 where it is transferred to a lysine residue on the targeted protein. The overall ubiquitination reaction causes protein degradation by proteasomes. 
 
Ubiquitin conjugating enyme is located in the cytosol.  To isolate fractions for ELISA assay, use a non-denaturing detergent lysis buffer such as Part  No. ELSP-1, or similar to lyze membranes and release a soluble cytosolic fraction.  The protocol associated with Part No ELSP-1 can be used to isolate cytosolic fractions for ELISA measurement.
 

Methods
Overview      
 
 
The included ELISA micro-strip plate is provided pre-coated with an a monoclonal capture antibody selective to the antigen.  Samples are pre-mixed with a biotin-linked detection antibody and streptavidin-HRP, which are then added to the plate.  The plate is washed after a 60 min incubation period.  Color reagents are added, resulting in a reaction with HRP that yields a blue colored solution.  A stop solution is applied to terminate the reaction, and the solution is measured at 450nm.


   Sandwich ELISA Methods to E2/UBCE                                                                                                                                                                                                      
 
ELISA Assay Steps
  1. Mix sample, biotinylated-detection antibody and streptavidin-HRP.
  2. Apply sample and antibody-HRP complex to ELISA plate for 60min at 37oC.Wash 5 times.
  3. Apply chromogens, incubate, then stop reaction.

 

 


E2/UBCE            
References                 1. Wiebel, Franziska F., and Wolf-H. Kunau. 1992. "The Pas2 protein essential for peroxisome biogenesis is related to ubiquitin
conjugating enzymes." Nature 359.6390, 73-76. 
2. Seufert, Wolfgang, Bruce Futcher, and Stefan Jentsch.1995. "Role of a ubiquitin-conjugating enzyme in degradation of S-and M-phase cyclins."  78-81.
3. Jahngen-Hodge, Jessica, et al. 1997. "Regulation of ubiquitin-conjugating enzymes by glutathione following oxidative stress." Journal of Biological Chemistry 272.45, 28218-28226.
4. Moraes, Trevor F., et al. 2001. "Crystal structure of the human ubiquitin conjugating enzyme complex, hMms2–hUbc13." Nature Structural & Molecular Biology 8.8, 669-673.
 

For research only. Not for Diagnostics.
Safety:  Stop solution contains acid.   Avoid ingestion, skin and eye contact.
Storage:  4°C. 6 months.
Shipping.  Overnight domestic delivery recommended with ice packs.  Also avaialble for international delivery; please inquire for shipping cost. 


 

Category Download Link
Protocol Manual click here
MSDS click here