Rat OB (Obestatin) ELISA Kit (RTFI01494)

SKU:
RTFI01494
€499

Description

Rat OB (Obestatin) ELISA Kit - Information

The Assay Genie Rat OB (Obestatin) ELISA Kit can assay for Rat OB (Obestatin) in the following samples: serum, blood, plasma, cell culture supernatant and other related supernatants and tissues.

How our Rat OB (Obestatin) ELISA Kits Work?

This Rat OB (Obestatin) ELISA Kit is based on Competitive-ELISA detection method. The microtiter plate provided in this kit has been pre-coated with analyte of interest. During the reaction, the analyte in the sample or standard competes with a fixed amount of target on the solid phase supporter for sites on the Biotinylated Detection Antibody specific to analyte. Excess conjugate and unbound sample or standard are washed from the plate, and HRP-Streptavidin (SABC) is added to each microplate well and incubated. TMB substrate solution is then added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the colour change is measured spectrophotometrically at a wavelength of 450nm. The concentration of target in the samples is then determined by comparing the OD of the samples to the standard curve.

Rat OB (Obestatin) ELISA Kit Data

Product Code

RTFI01494

Alias

Obestatin ELISA Kit

Detection method

Competitive ELISA, Coated with Antibody

Application

This immunoassay kit allows for the in vitro quantitative determination of Rat OB (Obestatin) concentrations in serum plasma and other biological fluids.

Size

96T

Range

15.625-1000pg/ml

Sensitivity

< 9.375pg/ml

Storage

4'C for 6 months

Recovery

Matrices listed below were spiked with certain level of Rat OB (Obestatin) and the recovery rates were calculated by comparing the measured value to the expected amount of Rat OB (Obestatin) in samples.

Not Available
Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Rat OB (Obestatin) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Not Available
CV(%)

Intra-Assay: CV<8%
Inter-Assay: CV<10%

Note

For Research Use Only

Rat OB (Obestatin) ELISA Kit Protocol

The below protocol is a sample protocol for a Rat OB (Obestatin) ELISA Kit. Competitive ELISA kits allow for the detection and quantification of an analyte in a sample. This Rat OB (Obestatin) ELISA Kit allows the researcher to calculate the amount of Rat OB (Obestatin) in their sample. Equilibrate the TMB substrate for at least 30 min at 37°C before use. When diluting samples and reagents, they must be mixed completely and evenly. It is recommended to plot a standard curve for each test.

Kit Protocol:

1. Set standard, test sample and control (zero) wells on the pre-coated plate respectively, and then, record their positions. It is recommended to measure each standard and sample in duplicate. Wash plate 2 times before adding standard, sample and control (zero) wells!
2. Add Sample and Biotin-detection antibody: Add 50µL of Standard, Blank or Sample per well. The blank well is added with Sample Dilution Buffer. Immediately add 50 µL of biotin-labelled antibody working solution to each well. Cover with the plate sealer provided. Gently tap the plate to ensure thorough mixing. Incubate for 45 minutes at 37°C. (Solutions are added to the bottom of micro-ELISA plate well, avoid touching plate walls and foaming).
3. Wash: Aspirate each well and wash, repeating the process three times Wash by filling each well with Wash Buffer (approximately 350µL) using a squirt bottle, multi-channel pipette, manifold dispenser or automated washer. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Buffer by aspirating or decanting. Invert the plate and pat it against thick clean absorbent paper.
4. HRP-Streptavidin Conjugate(SABC): Add 100µL of SABC working solution to each well. Cover with a new Plate sealer. Incubate for 30minutes at 37°C.
5. Wash: Repeat the aspiration/wash process for five times.
6. TMB Substrate: Add 90µL of TMB Substrate to each well. Cover with a new Plate sealer. Incubate for about 10-20 minutes at 37°C. Protect from light. The reaction time can be shortened or extended according to the actual color change, but not more than 30minutes. When apparent gradient appeared in standard wells, you can terminate the reaction.
7. Stop: Add 50µL of Stop Solution to each well. Color turn to yellow immediately. The adding order of stop solution should be as the same as the substrate solution.
8. OD Measurement: Determine the optical density (OD Value) of each well at once, using a microplate reader set to 450 nm. You should open the microplate reader ahead, preheat the instrument, and set the testing parameters.

Rat OB (Obestatin) ELISA Kit components

96 Assays

Storage

ELISA Microplate(Dismountable) 8×12 strips 4°C for 6 months
Lyophilized Standard 2 4°C/-20°C
Sample/Standard Dilution Buffer 20ml 4°C
Biotin-labeled Antibody(Concentrated) 60ul 4°C (Protect from light)
Antibody Dilution Buffer 10ml 4°C
HRP-Streptavidin Conjugate(SABC) 120ul 4°C (Protect from light)
SABC Dilution Buffer 10ml 4°C
TMB Substrate 10ml 4°C (Protect from light)
Stop Solution 10ml 4°C
Wash Buffer(25X) 30ml 4°C
Plate Sealer 5 -

Other materials and equipment required:

The Assay Genie Rat OB (Obestatin) ELISA Kit will require other equipment and materials to carry out the assay. Please see list below for further details.

  • Microplate reader with 450 nm wavelength filter
  • Multichannel Pipette, Pipette, microcentrifuge tubes and disposable pipette tips
  • Incubator
  • Deionized or distilled water
  • Absorbent paper
  • Buffer resevoir

Sample Preparation

When carrying out an ELISA assay it is important to prepare your samples in order to achieve the best possible results. Below we have a list of procedures for the preparation of samples for different sample types.

Sample Type Protocol

Serum

If using serum separator tubes, allow samples to clot for 30 minutes at room temperature. Centrifuge for 10 minutes at 1,000x g. Collect the serum fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.

If serum separator tubes are not being used, allow samples to clot overnight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Remove serum and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.

Plasma

Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples at 4°C for 15 mins at 1000 × g within 30 mins of collection. Collect the plasma fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles. Note: Over haemolysed samples are not suitable for use with this kit.

Urine & Cerebrospinal Fluid

Collect the urine (mid-stream) in a sterile container, centrifuge for 20 mins at 2000-3000 rpm. Remove supernatant and assay immediately. If any precipitation is detected, repeat the centrifugation step. A similar protocol can be used for cerebrospinal fluid.

Cell culture supernatant

Collect the cell culture media by pipette, followed by centrifugation at 4°C for 20 mins at 1500 rpm. Collect the clear supernatant and assay immediately.

Cell lysates

Solubilize cells in lysis buffer and allow to sit on ice for 30 minutes. Centrifuge tubes at 14,000 x g for 5 minutes to remove insoluble material. Aliquot the supernatant into a new tube and discard the remaining whole cell extract. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C.

Tissue homogenates

The preparation of tissue homogenates will vary depending upon tissue type. Rinse tissue with 1X PBS to remove excess blood & homogenize in 20ml of 1X PBS (including protease inhibitors) and store overnight at ≤ -20°C. Two freeze-thaw cycles are required to break the cell membranes. To further disrupt the cell membranes you can sonicate the samples. Centrifuge homogenates for 5 mins at 5000xg. Remove the supernatant and assay immediately or aliquot and store at -20°C or -80°C.

Tissue lysates

Rinse tissue with PBS, cut into 1-2 mm pieces, and homogenize with a tissue homogenizer in PBS. Add an equal volume of RIPA buffer containing protease inhibitors and lyse tissues at room temperature for 30 minutes with gentle agitation. Centrifuge to remove debris. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C.

Breast Milk

Collect milk samples and centrifuge at 10,000 x g for 60 min at 4°C. Aliquot the supernatant and assay. For long term use, store samples at -80°C. Minimize freeze/thaw cycles.

UniProt Protein Function:ghrelin: a hormone that binds to the growth hormone secretagogue receptor type 1 (GHSR). Secreted by the stomach
UniProt Protein Details:

Protein type:Secreted, signal peptide; Cell development/differentiation; Secreted; Cell cycle regulation; Apoptosis

Cellular Component: axon; cytoplasm; cytosol; extracellular region; extracellular space

Molecular Function:G-protein-coupled receptor binding; ghrelin receptor binding; growth hormone-releasing hormone activity; hormone activity; protein tyrosine kinase activator activity

Biological Process: actin polymerization and/or depolymerization; activation of MAPK activity; adult feeding behavior; decidualization; dendrite development; elevation of cytosolic calcium ion concentration; G-protein coupled receptor protein signaling pathway; gastric acid secretion; hormone-mediated signaling; negative regulation of apoptosis; negative regulation of circadian sleep/wake cycle, REM sleep; negative regulation of endothelial cell proliferation; negative regulation of inflammatory response; negative regulation of insulin secretion; negative regulation of interleukin-1 beta production; negative regulation of interleukin-6 biosynthetic process; negative regulation of locomotion; negative regulation of tumor necrosis factor biosynthetic process; positive regulation of adrenocorticotropic hormone secretion; positive regulation of appetite; positive regulation of circadian sleep/wake cycle, non-REM sleep; positive regulation of cortisol secretion; positive regulation of growth hormone secretion; positive regulation of insulin secretion; positive regulation of response to food; positive regulation of synaptogenesis; regulation of cell proliferation; regulation of excitatory postsynaptic membrane potential; regulation of response to food; response to estrogen stimulus; response to hormone stimulus

NCBI Summary:endogenous ligand for the growth hormone secretagogue receptor (GHSR); involved in testicular function and GH release [RGD, Feb 2006]
UniProt Code:Q9QYH7
NCBI GenInfo Identifier:11067387
NCBI Gene ID:59301
NCBI Accession:NP_067701.1
UniProt Secondary Accession:Q9QYH7,Q9ET69,
UniProt Related Accession:Q9QYH7
Molecular Weight:13,048 Da
NCBI Full Name:appetite-regulating hormone preproprotein
NCBI Synonym Full Names:ghrelin/obestatin prepropeptide
NCBI Official Symbol:Ghrl  
NCBI Protein Information:appetite-regulating hormone
UniProt Protein Name:Appetite-regulating hormone
UniProt Synonym Protein Names:Growth hormone secretagogue; Growth hormone-releasing peptide; Motilin-related peptide
Protein Family:Appetite-regulating hormone
UniProt Gene Name:Ghrl  
UniProt Entry Name:GHRL_RAT
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Additional Information

Product type:
ELISA
Reactivity:
Rat
ELISA Type:
Competitive
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