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HSL (Phospho-Ser552)Colorimetric Cell-Based ELISA Kit (CBCAB00137)

SKU:
CBCAB00137
Product Type:
ELISA Kit
ELISA Type:
Cell Based Phospho Specific
Research Area:
Metabolism
Reactivity:
Human
Mouse
Rat
Detection Method:
Colorimetric
€960
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Description

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HSL (Phospho-Ser552)Colorimetric Cell-Based ELISA Kit

The Human HSL (Hormone-Sensitive Lipase) Phospho-Ser552 Colorimetric Cell-Based ELISA Kit is a powerful tool for measuring levels of phosphorylated Hormone-Sensitive Lipase at Serine 552 in cell lysates. This kit offers high specificity and sensitivity, ensuring accurate and reproducible results for a variety of research applications.Hormone-Sensitive Lipase is a key enzyme involved in the regulation of lipid metabolism and energy balance. Phosphorylation at Serine 552 is known to modulate its activity, making it a crucial target for studying cellular processes related to lipid metabolism, obesity, and metabolic disorders.

The ability to quantify phosphorylated HSL levels in cell lysates provides valuable insight into these pathways and facilitates the development of potential therapeutic interventions.The HSL Phospho-Ser552 Colorimetric Cell-Based ELISA Kit is a valuable tool for researchers studying lipid metabolism, obesity, and related disorders. With its high sensitivity and specificity, this kit offers reliable and reproducible results, allowing for in-depth analysis of cellular signaling pathways and potential therapeutic targets.

Product Name:HSL (Phospho-Ser552) Colorimetric Cell-Based ELISA
Product Code:CBCAB00137
ELISA Type:Cell-Based
Target:HSL (Phospho-Ser552)
Reactivity:Human, Mouse, Rat
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nm
Format:2 x 96-Well Microplates

The HSL (Phospho-Ser552) Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect HSL protein phosphorylation and expression profile in cells. The kit can be used for measuring the relative amounts of phosphorylated HSL in cultured cells as well as screening for the effects that various treatments, inhibitors (ie. siRNA or chemicals), or activators have on HSL phosphorylation.

Qualitative determination of HSL (Phospho-Ser552) concentration is achieved by an indirect ELISA format. In essence, HSL (Phospho-Ser552) is captured by HSL (Phospho-Ser552)-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: 3991, UniProt ID: Q05469, OMIM: 151750, Unigene: Hs.656980
Gene Symbol:LIPE
Sub Type:Phospho
UniProt Protein Function:HSL: hormone sensitive lipase is a lipolytic enzyme of the 'GDXG' family. Plays a rate limiting step in triglyceride lipolysis. In adipose tissue and heart, it primarily hydrolyzes stored triglycerides to free fatty acids, while in steroidogenic tissues, it principally converts cholesteryl esters to free cholesterol for steroid hormone production. Rapidly activated by cAMP-dependent phosphorylation under the influence of catecholamines. Dephosphorylation and inactivation are controlled by insulin.
UniProt Protein Details:

Protein type:EC 3.1.1.79; Lipase

Chromosomal Location of Human Ortholog: 19q13.2

Cellular Component: lipid particle

Molecular Function:protein binding

Biological Process: lipid catabolic process; protein amino acid phosphorylation

Disease: Abdominal Obesity-metabolic Syndrome 4

NCBI Summary:The protein encoded by this gene has a long and a short form, generated by use of alternative translational start codons. The long form is expressed in steroidogenic tissues such as testis, where it converts cholesteryl esters to free cholesterol for steroid hormone production. The short form is expressed in adipose tissue, among others, where it hydrolyzes stored triglycerides to free fatty acids. [provided by RefSeq, Jul 2008]
UniProt Code:Q05469
NCBI GenInfo Identifier:145559491
NCBI Gene ID:3991
NCBI Accession:Q05469.4
UniProt Secondary Accession:Q05469,Q3LRT2, Q6NSL7,
UniProt Related Accession:Q05469
Molecular Weight:84,128 Da
NCBI Full Name:Hormone-sensitive lipase
NCBI Synonym Full Names:lipase E, hormone sensitive type
NCBI Official Symbol:LIPE  
NCBI Official Synonym Symbols:HSL; LHS; AOMS4; FPLD6  
NCBI Protein Information:hormone-sensitive lipase
UniProt Protein Name:Hormone-sensitive lipase
Protein Family:Hormone-sensitive lipase
UniProt Gene Name:LIPE  
UniProt Entry Name:LIPS_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-HSL (Phospho-Ser552) Antibody, Anti-HSL 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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