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TCOF1 Colorimetric Cell-Based ELISA

SKU:
CBCAB01084
Product Type:
ELISA Kit
ELISA Type:
Cell Based
Reactivity:
Human
Mouse
Detection Method:
Colorimetric
€599
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Description

system_update_altDatasheetMSDS

TCOF1 Colorimetric Cell-Based ELISA

The TCOF1 (Treacle Ribosome Biogenesis Factor 1) Colorimetric Cell-Based ELISA Kit is a powerful tool for researchers looking to accurately quantify TCOF1 protein levels in cell lysates. This kit offers high sensitivity and specificity, allowing for reliable and reproducible results in a variety of experimental settings.TCOF1 is a key factor in ribosome biogenesis, essential for proper development of craniofacial structures. Mutations in TCOF1 have been linked to Treacher Collins syndrome, a rare genetic disorder characterized by facial deformities. Understanding the expression levels of TCOF1 can provide valuable insights into the molecular mechanisms underlying this condition, aiding in the development of potential treatments and interventions.

With the TCOF1 Colorimetric Cell-Based ELISA Kit, researchers can accurately measure TCOF1 levels in cell lysates, enabling further exploration of its role in ribosome biogenesis and craniofacial development. This kit is a valuable tool for studying TCOF1-related pathways and diseases, offering a comprehensive solution for quantitative analysis in cell-based research.

Product Name:TCOF1 Colorimetric Cell-Based ELISA
Product Code:CBCAB01084
ELISA Type:Cell-Based
Target:TCOF1
Reactivity:Human, Mouse
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nmStorage/Stability:4°C/6 Months
Format:96-Well Microplate

The TCOF1 Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect TCOF1 protein expression profile in cells. The kit can be used for measuring the relative amounts of TCOF1 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on TCOF1.

Qualitative determination of TCOF1 concentration is achieved by an indirect ELISA format. In essence, TCOF1 is captured by TCOF1-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: 6949, UniProt ID: Q13428, OMIM: 154500/606847, Unigene: Hs.519672/Hs.605019
Gene Symbol:TCOF1
Sub Type:None
UniProt Protein Function:treacle: May be involved in nucleolar-cytoplasmic transport. May play a fundamental role in early embryonic development, particularly in development of the craniofacial complex. May participate in certain stages of ribosome biogenesis. Defects in TCOF1 are the cause of Treacher Collins syndrome type 1 (TCS1). It is a form of Treacher Collins syndrome, a disorder of craniofacial development. Treacher Collins syndrome is characterized by a combination of bilateral downward slanting of the palpebral fissures, colobomas of the lower eyelids with a paucity of eyelashes medial to the defect, hypoplasia of the facial bones, cleft palate, malformation of the external ears, atresia of the external auditory canals, and bilateral conductive hearing loss. 8 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:

Protein type:Transcription, coactivator/corepressor; RNA-binding; Nucleolus

Chromosomal Location of Human Ortholog: 5q32

Cellular Component: cytoplasm; nucleolus; nucleus

Molecular Function:protein binding; transporter activity

Biological Process: transport; transcription of nuclear rRNA large RNA polymerase I transcript; skeletal development

Disease: Treacher Collins Syndrome 1

NCBI Summary:This gene encodes a nucleolar protein with a LIS1 homology domain. The protein is involved in ribosomal DNA gene transcription through its interaction with upstream binding factor (UBF). Mutations in this gene have been associated with Treacher Collins syndrome, a disorder which includes abnormal craniofacial development. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]
UniProt Code:Q13428
NCBI GenInfo Identifier:302393806
NCBI Gene ID:6949
NCBI Accession:Q13428.3
UniProt Secondary Accession:Q13428,Q6SC72, Q7Z5W9, Q96A52, Q99408, Q99860, A0JLU0 B4E111,
UniProt Related Accession:Q13428
Molecular Weight:1488
NCBI Full Name:Treacle protein
NCBI Synonym Full Names:Treacher Collins-Franceschetti syndrome 1
NCBI Official Symbol:TCOF1  
NCBI Official Synonym Symbols:TCS; MFD1; TCS1; treacle  
NCBI Protein Information:treacle protein; Treacher Collins syndrome protein; nucleolar trafficking phosphoprotein
UniProt Protein Name:Treacle protein
UniProt Synonym Protein Names:Treacher Collins syndrome protein
Protein Family:Treacle protein
UniProt Gene Name:TCOF1  
UniProt Entry Name:TCOF_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-TCOF1 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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