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ZNF24 Colorimetric Cell-Based ELISA

SKU:
CBCAB00977
Product Type:
ELISA Kit
ELISA Type:
Cell Based
Research Area:
Epigenetics and Nuclear Signaling
Reactivity:
Human
Mouse
Rat
Detection Method:
Colorimetric
$719
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Description

system_update_altDatasheet

ZNF24 Colorimetric Cell-Based ELISA

The ZNF24 Colorimetric Cell-based ELISA Kit is a cutting-edge assay designed for the detection and quantification of ZNF24 protein levels in cell lysates and tissue homogenates. This kit offers superior sensitivity and accuracy, allowing researchers to obtain precise and reliable results for their studies.ZNF24 is a key transcription factor that plays a crucial role in gene regulation and cell differentiation. Dysregulation of ZNF24 has been associated with various diseases, including cancer and developmental disorders.

By measuring ZNF24 levels, researchers can gain valuable insights into the molecular mechanisms underlying these conditions and identify potential therapeutic targets.With easy-to-follow protocols and quick assay turnaround times, the ZNF24 Colorimetric Cell-based ELISA Kit is the perfect tool for investigating the role of ZNF24 in cellular processes and disease pathology. Trust in this innovative kit for robust and reproducible data in your research endeavors.

Product Name:ZNF24 Colorimetric Cell-Based ELISA
Product Code:CBCAB00977
ELISA Type:Cell-Based
Target:ZNF24
Reactivity:Human, Mouse, Rat
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nmStorage/Stability:4°C/6 Months
Format:96-Well Microplate

The ZNF24 Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect ZNF24 protein expression profile in cells. The kit can be used for measuring the relative amounts of ZNF24 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on ZNF24.

Qualitative determination of ZNF24 concentration is achieved by an indirect ELISA format. In essence, ZNF24 is captured by ZNF24-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: 7572, UniProt ID: P17028, OMIM: 194534, Unigene: Hs.514802
Gene Symbol:ZNF24
Sub Type:None
UniProt Protein Function:ZNF24: a probable transcriptional regulator of the krueppel C2H2-type zinc-finger protein family.
UniProt Protein Details:

Protein type:DNA-binding; Transcription factor; C2H2-type zinc finger protein

Chromosomal Location of Human Ortholog: 18q12

Cellular Component: nucleoplasm; nucleus

Molecular Function:protein binding; DNA binding; zinc ion binding; sequence-specific DNA binding; transcription factor activity

Biological Process: myelination; transcription, DNA-dependent; negative regulation of transcription, DNA-dependent

UniProt Code:P17028
NCBI GenInfo Identifier:160376173
NCBI Gene ID:7572
NCBI Accession:P17028.4
UniProt Secondary Accession:P17028,O14754, Q53YE4, Q6ICR5, Q8IZN4,
UniProt Related Accession:P17028
Molecular Weight:368
NCBI Full Name:Zinc finger protein 24
NCBI Synonym Full Names:zinc finger protein 24
NCBI Official Symbol:ZNF24  
NCBI Official Synonym Symbols:KOX17; RSG-A; ZNF191; ZSCAN3; Zfp191  
NCBI Protein Information:zinc finger protein 24; zinc finger protein 191; lacks zinc finger domain; zinc finger protein KOX17; zinc finger protein 24 (KOX 17); retinoic acid suppression protein A; zinc finger and SCAN domain-containing protein 3
UniProt Protein Name:Zinc finger protein 24
UniProt Synonym Protein Names:Retinoic acid suppression protein A; RSG-A; Zinc finger and SCAN domain-containing protein 3; Zinc finger protein 191; Zinc finger protein KOX17
Protein Family:Zinc finger protein
UniProt Gene Name:ZNF24  
UniProt Entry Name:ZNF24_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-ZNF24 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.)

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