null

VPS72 Colorimetric Cell-Based ELISA

SKU:
CBCAB01118
Product Type:
ELISA Kit
ELISA Type:
Cell Based
Research Area:
Epigenetics and Nuclear Signaling
Reactivity:
Human
Mouse
Detection Method:
Colorimetric
$719
Frequently bought together:

Description

system_update_altDatasheet

VPS72 Colorimetric Cell-Based ELISA

The VPS72 Colorimetric Cell-Based ELISA Kit offered by AssayGenie is specifically designed for the accurate and reliable detection of VPS72 levels in cell lysates. This kit features high sensitivity and specificity, allowing for precise measurements of VPS72 expression in a variety of cell types and experimental conditions.VPS72 is a critical component of the SWI/SNF chromatin remodeling complex, playing a crucial role in regulating gene expression and chromatin structure.

Dysregulation of VPS72 has been implicated in various diseases, including cancer and neurological disorders, making it a valuable target for research and drug development.With the VPS72 Colorimetric Cell-Based ELISA Kit, researchers can confidently measure VPS72 levels in cell lysates, providing valuable insights into its function and potential therapeutic applications. Trust AssayGenie for accurate and reproducible results in your VPS72 research.

Product Name:VPS72 Colorimetric Cell-Based ELISA
Product Code:CBCAB01118
ELISA Type:Cell-Based
Target:VPS72
Reactivity:Human, Mouse
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nmStorage/Stability:4°C/6 Months
Format:96-Well Microplate

The VPS72 Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect VPS72 protein expression profile in cells. The kit can be used for measuring the relative amounts of VPS72 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on VPS72.

Qualitative determination of VPS72 concentration is achieved by an indirect ELISA format. In essence, VPS72 is captured by VPS72-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: 6944, UniProt ID: Q15906, OMIM: 600607, Unigene: Hs.2430
Gene Symbol:VPS72
Sub Type:None
UniProt Protein Function:VPS72: Could be a DNA-binding transcriptional regulator. May be involved in chromatin modification and remodeling. Belongs to the VPS72/YL1 family.
UniProt Protein Details:

Protein type:DNA-binding

Chromosomal Location of Human Ortholog: 1q21

Cellular Component: nucleoplasm; nucleus; protein complex

Molecular Function:DNA binding; protein binding

Biological Process: establishment and/or maintenance of chromatin architecture; histone exchange; negative regulation of transcription from RNA polymerase II promoter; somatic stem cell maintenance; transcription, DNA-dependent

NCBI Summary:The protein encoded by this gene is a shared subunit of two multi-component complexes, the histone acetyltransferase complex TRRAP/TIP60 as well as the chromatin remodeling SRCAP-containing complex. The TRRAP/TIP60 complex acetylates nucleosomal histones important for transcriptional regulation, double strand DNA break repair and apoptosis. The SRCAP-containing complex catalyzes the exchange of histone H2A with the histone variant Htz1 (H2AFZ) into nucleosomes. This protein may be responsible for binding H2AFZ, which has a role in chromosome segregation. This protein may also have a role in regulating long-term hematopoietic stem cell activity. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012]
UniProt Code:Q15906
NCBI GenInfo Identifier:2499159
NCBI Gene ID:6944
NCBI Accession:Q15906.1
UniProt Secondary Accession:Q15906,Q53GJ2, Q5U0R4, A6NLK9, A6PW55,
UniProt Related Accession:Q15906
Molecular Weight:41,848 Da
NCBI Full Name:Vacuolar protein sorting-associated protein 72 homolog
NCBI Synonym Full Names:vacuolar protein sorting 72 homolog
NCBI Official Symbol:VPS72  
NCBI Official Synonym Symbols:YL1; CFL1; Swc2; YL-1; TCFL1  
NCBI Protein Information:vacuolar protein sorting-associated protein 72 homolog
UniProt Protein Name:Vacuolar protein sorting-associated protein 72 homolog
UniProt Synonym Protein Names:Protein YL-1; Transcription factor-like 1
Protein Family:Vacuolar protein sorting-associated protein
UniProt Gene Name:VPS72  
UniProt Entry Name:VPS72_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-VPS72 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