Human Phospho-Cyclin B1 (S126) and Total Cyclin B1 ELISA

RayBio® Human Phospho-Cyclin B1 (Ser126) and Total Cyclin B1 ELISA Kit. This assay semi-quantitatively measures Cyclin B1 phosphorylated at Serine-126 as well as total Cyclin B1 in cell lysate samples.

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Code:
PEL-CYCLINB1-S126-T
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Product Description

Specifications

Size 1 Plate Kit, 2 Plate Kit, 5 Plate Kit
Species Human
Targets Detected Cyclin B1
Protein Name / Synonyms G2/mitotic-specific cyclin-B1
Specificity The antibody pair provided in this kit recognizes Human Cyclin B1 phosphorylated at site Serine-126 as well as total Cyclin B1.
Accession Number P14635
Gene Symbols CCNB1
Gene Id 891
Quantitative/Semi-Quantitative Semi-Quantitative
Compatible Sample Types Tissue Lysates, Cell Lysates
Solid Support 96-well Microplate
Method Of Detection Colorimetric
Design Principle Sandwich-based
Research Area Post-Translational Modifications, Phosphorylation, AMPK Signaling, Cell Cycle, DNA Damage

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Product Features

  • Rapidly measure phosphorylated protein in lysates
  • Screen numerous different cell lysates without performing a Western Blot analysis
  • Minimal hands-on time, convenient, and non-radioactive material

Application Notes

Kit Components
  • Pre-Coated 96-well Strip Microplate
  • Wash Buffer
  • Anti-Phospho Antibody
  • HRP-Conjugated Secondary Antibody
  • Assay Diluent
  • TMB One-Step Substrate
  • Stop Solution
  • Lysis Buffer
  • Positive Control Sample
Other Materials Required
  • Distilled or deionized water
  • 100 ml and 1 liter graduated cylinders
  • Tubes to prepare sample dilutions
  • Protease and Phosphatase inhibitors
  • Precision pipettes to deliver 2 µl to 1 ml volumes
  • Adjustable 1-25 ml pipettes for reagent preparation
  • Benchtop rocker or shaker
  • Microplate reader capable of measuring absorbance at 450 nm
Protocol Outline
  1. Prepare all reagents and samples as instructed in the manual.
  2. Add 100 µl of sample or positive control to each well.
  3. Incubate 2.5 h at RT or O/N at 4 °C.
  4. Add 100 µl of prepared primary antibody to each well.
  5. Incubate 1 h at RT.
  6. Add 100 µl of prepared 1X HRP-Streptavidin to each well.
  7. Incubate 1 h at RT.
  8. Add 100 µl of TMB One-Step Substrate Reagent to each well.
  9. Incubate 30 min at RT.
  10. Add 50 µl of Stop Solution to each well.
  11. Read at 450 nm immediately.

Typical Data

Positive Control
HeLa cells were treated with Nocodazole at 37°C for 20 hours. Cells were solubilzed at 4 x 107 cells/ml in Cell Lysate Buffer. Serial dilutions of lysates were analyzed in this ELISA (see Reagent Preparation step 4).
Nocodazole Stimulation of HeLa Cell Lines
HeLa cells were untreated or treated with Nocodazole for 20 hours. Cell lysates were analyzed using this phosphoELISA and Western Blot. 


Storage/Stability

Upon receipt, the kit should be stored at –20°C. Please use within 6 months from the date of shipment.
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