null

CEBPZ Colorimetric Cell-Based ELISA

SKU:
CBCAB01062
Product Type:
ELISA Kit
ELISA Type:
Cell Based
Research Area:
Epigenetics and Nuclear Signaling
Reactivity:
Human
Detection Method:
Colorimetric
$719
Frequently bought together:

Description

system_update_altDatasheetMSDS

CEBPZ Colorimetric Cell-Based ELISA

The CEBPZ Colorimetric Cell-Based ELISA Kit is a cutting-edge product designed for the accurate measurement of CCAAT/enhancer-binding protein zeta (CEBPZ) levels in cell-based assays. This kit offers high sensitivity and specificity, ensuring precise and reliable results for a variety of research applications.CEBPZ is a key transcription factor that regulates gene expression and plays a critical role in various cellular processes, including cell growth, differentiation, and inflammation. Dysregulation of CEBPZ has been linked to several diseases, such as cancer, autoimmune disorders, and metabolic syndromes, making it a valuable target for further investigation and therapeutic development.

The CEBPZ Colorimetric Cell-Based ELISA Kit provides researchers with a powerful tool to study the function of CEBPZ in cellular signaling pathways and disease mechanisms. With its easy-to-use protocol and robust performance, this kit is an essential addition to any laboratory looking to advance their understanding of molecular biology and pathology.

Product Name:CEBPZ Colorimetric Cell-Based ELISA
Product Code:CBCAB01062
ELISA Type:Cell-Based
Target:CEBPZ
Reactivity:Human
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nmStorage/Stability:4°C/6 Months
Format:96-Well Microplate

The CEBPZ Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect CEBPZ protein expression profile in cells. The kit can be used for measuring the relative amounts of CEBPZ in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on CEBPZ.

Qualitative determination of CEBPZ concentration is achieved by an indirect ELISA format. In essence, CEBPZ is captured by CEBPZ-specific primary antibodies while the HRP-conjugated secondary antibodies bind the Fc region of the primary antibody. Through this binding, the HRP enzyme conjugated to the secondary antibody can catalyze a colorimetric reaction upon substrate addition. Due to the qualitative nature of the Cell-Based ELISA, multiple normalization methods are needed:

1. A monoclonal antibody specific for human GAPDH is included to serve as an internal positive control in normalizing the target absorbance values.
2. Following the colorimetric measurement of HRP activity via substrate addition, the Crystal Violet whole-cell staining method may be used to determine cell density. After staining, the results can be analysed by normalizing the absorbance values to cell amounts, by which the plating difference can be adjusted.
Database Information:Gene ID: 10153, UniProt ID: Q03701, OMIM: 612828, Unigene: Hs.135406
Gene Symbol:CEBPZ
Sub Type:None
UniProt Protein Function:C/EBP-zeta: Stimulates transcription from the HSP70 promoter. Belongs to the CBF/MAK21 family.
UniProt Protein Details:

Protein type:Transcription factor; RNA-binding

Chromosomal Location of Human Ortholog: 2p22.2

Molecular Function:DNA binding

Biological Process: positive regulation of transcription from RNA polymerase II promoter; transcription from RNA polymerase II promoter

NCBI Summary:This gene belongs to the CEBP family. The encoded protein plays a role in cellular response to environmental stimuli through a transcriptional process that involves heat shock factors, conserved DNA elements (heat shock elements or HSEs) and CCAAT boxes. The protein acts as a DNA-binding transcriptional activator and regulates the heat-shock protein 70 (HSP70) promoter in a CCAAT-dependent manner. The protein is also involved in cell growth and differentiation, particularly, hematopoietic differentiation. Methylation of the promoter of this gene or mutations within the gene may be correlated with occurance of acute myeloid leukemia (AML). [provided by RefSeq, Jun 2016]
UniProt Code:Q03701
NCBI GenInfo Identifier:308153621
NCBI Gene ID:10153
NCBI Accession:Q03701.3
UniProt Secondary Accession:Q03701,Q8NE75,
UniProt Related Accession:Q03701
Molecular Weight:120,974 Da
NCBI Full Name:CCAAT/enhancer-binding protein zeta
NCBI Synonym Full Names:CCAAT/enhancer binding protein zeta
NCBI Official Symbol:CEBPZ  
NCBI Official Synonym Symbols:CBF; CBF2; NOC1; HSP-CBF  
NCBI Protein Information:CCAAT/enhancer-binding protein zeta
UniProt Protein Name:CCAAT/enhancer-binding protein zeta
UniProt Synonym Protein Names:CCAAT-box-binding transcription factor; CBF; CCAAT-binding factor
Protein Family:CCAAT/enhancer-binding protein
UniProt Gene Name:CEBPZ  
UniProt Entry Name:CEBPZ_HUMAN
ComponentQuantity
96-Well Cell Culture Clear-Bottom Microplate2 plates
10X TBS24 mL
Quenching Buffer24 mL
Blocking Buffer50 mL
15X Wash Buffer50 mL
Primary Antibody Diluent12 mL
100x Anti-Phospho Target Antibody 60 µL
100x Anti-Target Antibody60 µL
Anti-GAPDH Antibody60 µL
HRP-Conjugated Anti-Rabbit IgG Antibody12 mL
HRP-Conjugated Anti-Mouse IgG Antibody12 mL
SDS Solution12 mL
Stop Solution24 mL
Ready-to-Use Substrate12 mL
Crystal Violet Solution12 mL
Adhesive Plate Seals2 seals

The following materials and/or equipment are NOT provided in this kit but are necessary to successfully conduct the experiment:

  • Microplate reader able to measure absorbance at 450 nm and/or 595 nm for Crystal Violet Cell Staining (Optional)
  • Micropipettes with capability of measuring volumes ranging from 1 µL to 1 ml
  • 37% formaldehyde (Sigma Cat# F-8775) or formaldehyde from other sources
  • Squirt bottle, manifold dispenser, multichannel pipette reservoir or automated microplate washer
  • Graph paper or computer software capable of generating or displaying logarithmic functions
  • Absorbent papers or vacuum aspirator
  • Test tubes or microfuge tubes capable of storing ≥1 ml
  • Poly-L-Lysine (Sigma Cat# P4832 for suspension cells)
  • Orbital shaker (optional)
  • Deionized or sterile water

*Note: Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.

StepProcedure
1.Seed 200 µL of 20,000 adherent cells in culture medium in each well of a 96-well plate. The plates included in the kit are sterile and treated for cell culture. For suspension cells and loosely attached cells, coat the plates with 100 µL of 10 µg/ml Poly-L-Lysine (not included) to each well of a 96-well plate for 30 minutes at 37°C prior to adding cells.
2.Incubate the cells for overnight at 37°C, 5% CO2.
3.Treat the cells as desired.
4.Remove the cell culture medium and rinse with 200 µL of 1x TBS, twice.
5.Fix the cells by incubating with 100 µL of Fixing Solution for 20 minutes at room temperature. The 4% formaldehyde is used for adherent cells and 8% formaldehyde is used for suspension cells and loosely attached cells.
6.Remove the Fixing Solution and wash the plate 3 times with 200 µL 1x Wash Buffer for five minutes each time with gentle shaking on the orbital shaker. The plate can be stored at 4°C for a week.
7.Add 100 µL of Quenching Buffer and incubate for 20 minutes at room temperature.
8.Wash the plate 3 times with 1x Wash Buffer for 5 minutes each time.
9.Add 200 µL of Blocking Buffer and incubate for 1 hour at room temperature.
10. Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time.
11.Add 50 µL of 1x primary antibodies (Anti-CEBPZ Antibody and/or Anti-GAPDH Antibody) to the corresponding wells, cover with Parafilm and incubate for 16 hours (overnight) at 4°C. If the target expression is known to be high, incubate for 2 hours at room temperature.
12.Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time.
13.Add 50 µL of 1x secondary antibodies (HRP-Conjugated AntiRabbit IgG Antibody or HRP-Conjugated Anti-Mouse IgG Antibody) to corresponding wells and incubate for 1.5 hours at room temperature.
14.Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time.
15.Add 50 µL of Ready-to-Use Substrate to each well and incubate for 30 minutes at room temperature in the dark.
16.Add 50 µL of Stop Solution to each well and read OD at 450 nm immediately using the microplate reader.

(Additional Crystal Violet staining may be performed if desired – details of this may be found in the kit technical manual.)

Related Products