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SEPT1 Colorimetric Cell-Based ELISA

SKU:
CBCAB01167
Product Type:
ELISA Kit
ELISA Type:
Cell Based
Research Area:
Cell Cycle
Reactivity:
Human
Mouse
Rat
Detection Method:
Colorimetric
€599
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Description

system_update_altDatasheetMSDS

SEPT1 Colorimetric Cell-Based ELISA

The SEPT1 Colorimetric Cell-Based ELISA Kit is a cutting-edge assay designed for the accurate detection of SEPT1 levels in cell culture supernatants. This kit offers high sensitivity and specificity, providing reliable and reproducible results for researchers studying the role of SEPT1 in various biological processes.SEPT1, a member of the septin family of GTP-binding proteins, plays a crucial role in cell division, cytoskeletal organization, and membrane dynamics.

Dysregulation of SEPT1 has been implicated in various diseases, including cancer, neurodegenerative disorders, and infectious diseases. Therefore, the SEPT1 Colorimetric Cell-Based ELISA Kit is an essential tool for researchers investigating the function of SEPT1 and its potential as a therapeutic target.

Product Name:SEPT1 Colorimetric Cell-Based ELISA
Product Code:CBCAB01167
ELISA Type:Cell-Based
Target:44440
Reactivity:Human, Mouse, Rat
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nmStorage/Stability:4°C/6 Months
Format:96-Well Microplate

The SEPT1 Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect SEPT1 protein expression profile in cells. The kit can be used for measuring the relative amounts of SEPT1 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on SEPT1.

Qualitative determination of 37135 concentration is achieved by an indirect ELISA format. In essence, 37135 is captured by 37135-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: 1731, UniProt ID: Q8WYJ6, OMIM: 612897, Unigene: Hs.632176
Gene Symbol:44440
Sub Type:None
UniProt Protein Function:SEPT1: Filament-forming cytoskeletal GTPase. May play a role in cytokinesis (Potential). Belongs to the septin family. 2 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:

Protein type:Cell cycle regulation; Hydrolase; Cytoskeletal

Chromosomal Location of Human Ortholog: 16p11.1

Molecular Function:protein binding

NCBI Summary:This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 2012]
UniProt Code:Q8WYJ6
NCBI GenInfo Identifier:20178107
NCBI Gene ID:1731
NCBI Accession:Q8WYJ6.2
UniProt Secondary Accession:Q8WYJ6,Q658T1, Q8NEZ1, Q96EL4, Q9H285, B4DVE6,
UniProt Related Accession:Q8WYJ6
Molecular Weight:18,354 Da
NCBI Full Name:Septin-1
NCBI Synonym Full Names:septin 1
NCBI Official Symbol:SEPT1  
NCBI Official Synonym Symbols:LARP; SEP1; DIFF6; PNUTL3  
NCBI Protein Information:septin-1
UniProt Protein Name:Septin-1
UniProt Synonym Protein Names:LARP; Peanut-like protein 3; Serologically defined breast cancer antigen NY-BR-24
UniProt Gene Name:SEPT1  
UniProt Entry Name:SEPT1_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-37135 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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