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TAL-1 Colorimetric Cell-Based ELISA Kit

SKU:
CBCAB00879
Product Type:
ELISA Kit
ELISA Type:
Cell Based
Research Area:
Developmental Biology
Reactivity:
Human
Mouse
Detection Method:
Colorimetric
€599
Frequently bought together:

Description

system_update_altDatasheetMSDS

TAL-1 Colorimetric Cell-Based ELISA Kit

The TAL-1 Colorimetric Cell-Based ELISA Kit is a powerful tool for researchers looking to accurately quantify T-cell acute lymphoblastic leukemia 1 (TAL-1) levels in cell lysates. This kit offers high sensitivity and specificity, ensuring precise and reliable results for a variety of research applications.TAL-1 is a transcription factor that plays a critical role in T-cell development and differentiation. Dysregulation of TAL-1 has been implicated in the pathogenesis of T-cell acute lymphoblastic leukemia, making it an important biomarker for studying and treating this disease.

With the TAL-1 Colorimetric Cell-Based ELISA Kit, researchers can confidently measure TAL-1 levels in cell lysates, helping to advance our understanding of T-cell leukemia and potentially leading to the development of new targeted therapies.

Product Name:TAL-1 Colorimetric Cell-Based ELISA
Product Code:CBCAB00879
ELISA Type:Cell-Based
Target:TAL-1
Reactivity:Human, Mouse
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nmStorage/Stability:4°C/6 Months
Format:96-Well Microplate

The TAL-1 Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect TAL-1 protein expression profile in cells. The kit can be used for measuring the relative amounts of TAL-1 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on TAL-1.

Qualitative determination of TAL-1 concentration is achieved by an indirect ELISA format. In essence, TAL-1 is captured by TAL-1-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: 6886, UniProt ID: P17542, OMIM: 187040, Unigene: Hs.705618/Hs.720349
Gene Symbol:TAL1
Sub Type:None
UniProt Protein Function:TAL1: a basic helix-loop-helix transcription. Regulates differentiation and survival during hemopoiesis. Implicated in the genesis of hemopoietic malignancies. It may play an important role in hemopoietic differentiation. Serves as a positive regulator of eryhtroid differentiation. Mutations are associated with T-cell leukemia and melanoma. Binds to the LIM domain containing protein Rhombotin-2.
UniProt Protein Details:

Protein type:DNA-binding; Oncoprotein; Transcription factor

Chromosomal Location of Human Ortholog: 1p32

Cellular Component: histone deacetylase complex; nuclear chromatin; nucleus; transcription factor complex

Molecular Function:chromatin binding; enzyme binding; histone deacetylase binding; protein binding; transcription factor activity

Biological Process: basophil differentiation; cell fate commitment; embryonic hemopoiesis; erythrocyte differentiation; hemopoiesis; megakaryocyte differentiation; positive regulation of cell division; positive regulation of chromatin assembly or disassembly; positive regulation of erythrocyte differentiation; positive regulation of mitotic cell cycle; positive regulation of protein complex assembly; positive regulation of transcription from RNA polymerase II promoter; positive regulation of transcription, DNA-dependent; regulation of transcription from RNA polymerase II promoter

Disease: Leukemia, Acute Lymphoblastic

UniProt Code:P17542
NCBI GenInfo Identifier:134305
NCBI Gene ID:6886
NCBI Accession:P17542.2
UniProt Secondary Accession:P17542,D3DQ24,
UniProt Related Accession:P17542
Molecular Weight:16,548 Da
NCBI Full Name:T-cell acute lymphocytic leukemia protein 1
NCBI Synonym Full Names:TAL bHLH transcription factor 1, erythroid differentiation factor
NCBI Official Symbol:TAL1  
NCBI Official Synonym Symbols:SCL; TCL5; tal-1; bHLHa17  
NCBI Protein Information:T-cell acute lymphocytic leukemia protein 1
UniProt Protein Name:T-cell acute lymphocytic leukemia protein 1
UniProt Synonym Protein Names:Class A basic helix-loop-helix protein 17; bHLHa17; Stem cell protein; T-cell leukemia/lymphoma protein 5
Protein Family:Transaldolase
UniProt Gene Name:TAL1  
UniProt Entry Name:TAL1_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-TAL-1 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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