Kontakt
+1 (314) 370-6046 oderKontakt
Visit our English Website
Antibodies.com LogoAntibodies.com Logo
Einloggen / AnmeldenMein Konto
0

Maus M6PR (cation independent) Kit Elisa (A312992)

Standard Curve - Mouse M6PR (cation independent) ELISA Kit (A312992) - Antibodies.com
90-Minuten-ELISA
$525
100% Qualitätsgarantie
Preis-Match-Garantie

Versandkosten
$40
Vorlaufzeit
Lieferung in 7-9 Werktagen

Telefon
+1 (314) 370-6046
Mo bis Frei, 8am - 4pm AST
Email
orders@antibodies.com

Produktname
Mouse M6PR (cation independent) ELISA Kit
Beschreibung
Mouse M6PR (cation independent) ELISA Kit is a 90 minute sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse M6PR (cation independent) in serum, plasma, and other biological fluids.
Assay-Typ
Sandwich (quantitative)
Assay-Prinzip
Mouse M6PR (cation independent) ELISA Kit (A312992) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse M6PR (cation independent) in serum, plasma or other biological fluids. An antibody specific for M6PR (cation independent) has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the M6PR (cation independent) present in each sample is bound to the wells by the immobilized antibody. Biotinylated Anti-M6PR (cation independent) Antibody, which also binds the M6PR (cation independent) present in each sample, and Streptavidin-HRP, which binds the Biotinylated Anti-M6PR (cation independent) Antibody, are added and the microtiter plate is incubated. Following incubation, unbound Biotinylated Anti-M6PR (cation independent) Antibody and unbound Streptavidin-HRP are removed by washing, and two substrate solutions are added to the wells. Color develops in proportion to the amount of M6PR (cation independent) captured in each well. The color development is stopped by addition of stop solution which changes the color from blue to yellow and the intensity of the color is then measured. The concentration of M6PR (cation independent) in the samples can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.
Plattform
Pre-coated Microplate (12 x 8 well strips)
Nachweismethode
Colorimetric
Instrument
Colorimetric Microplate Reader
Probentyp
Serum, plasma or other biological fluids.
Sensitivität
0.56 ng/L
Detektionsbereich
15-240 ng/L
Testdauer
1h 30m
Reaktivität
Mouse
Precision
Intra-assay CV: < 8%, Inter-assay CV: < 10%
Allgemeine Hinweise
Information online is representative. Always refer to the Product Manual inside the kit.
Lagerung
Store at +4°C. Do not use past expiration date!
Synonyms
300 kDa mannose 6 phosphate receptor, 300 kDa mannose 6-phosphate receptor, Cation independent mannose 6 phosphate receptor, Cation-independent mannose-6-phosphate receptor, CD222, CD222 antigen, CI Man 6 P receptor, CI Man-6-P receptor, CI MPR, CI-M6PR, CI-MPR, CIMPR, IGF 2 receptor, IGF 2R, IGF II receptor, IGF-II receptor, IGF2 receptor, Igf2r, Insulin like growth factor 2 receptor, Insulin like growth factor II receptor, Insulin-like growth factor 2 receptor, Insulin-like growth factor II receptor, M6P R, M6P/IGF2 receptor, M6P/IGF2R, M6PR, mannose 6 phosphate receptor, mannose 6 phosphate receptor, cation independent, MPR 300, MPR300, MPRI, MPRI_HUMAN
Haftungsausschluss
Dieses Produkt ist nur für Forschungszwecke bestimmt. Es ist nicht für diagnostische oder therapeutische Zwecke bestimmt.
Kit Components
Item Quantity Storage
Pre-Coated 96 Well Microplate 12 x 8 Well Strips +4°C
Standard Solution 500µl +4°C
Standard Diluent 3ml +4°C
Biotinylated Detection Antibody 1ml +4°C
Streptavidin-HRP 6ml +4°C
Wash Buffer (25X) 20ml +4°C
Substrate Solution A 6ml +4°C
Substrate Solution B 6ml +4°C
Stop Solution 6ml +4°C
Plate Sealers 5 Adhesive Strips -
Foil Pouch 1 Zip-Sealed Pouch -
Required Materials
The following materials are not included in the kit, but are required to run this assay:
  • Microplate reader capable of measuring absorbance at 450nm ± 10nm.
  • Squirt bottle, multichannel pipette reservoir, or automated microplate washer.
  • Graph paper or computer software capable of generating logarithmic functions.
  • Test tubes and Eppendorf tubes to prepare standards and samples.
  • Multi- and single-channel pipettes and sterile pipette tips.
  • Deionized or distilled water.
  • Absorbent paper towels.
  • 37°C incubator.
Important Notes
  • Samples cannot be diluted for use with this kit. Owing to the material used to prepare the kit, sample matrix interference may falsely depress the specificity and accuracy of the assay.
  • Sample concentrations should be estimated before being used in the assay. If the sample concentration is not within the range of the standard curve, users must contact us to determine the optimal sample for their experiments.
  • Samples containing Sodium Azide (NaN3) cannot be used in this assay. NaN3 inhibits the activity of Horseradish Peroxidase (HRP) which is used in the detection step.
Bring all reagents and samples to room temperature before use.
We recommend that all standards, controls, and samples be assayed in duplicate.
Step 1
Prepare all reagents, samples, and working standards as directed in the Product Manual.
Step 2
Determine the number of microplate strips required for the assay and insert them into the plate frame. Unused strips should be stored in the foil pouch at +4°C.
Step 3
Add 50μl of standard to the standard wells.
Step 4
Add 40μl of samples to the sample wells.
Step 5
Add 10μl of Biotinylated Detection Antibody to sample wells (but not to the standard wells).
Step 6
Add 50μl of Streptavidin-HRP to sample wells and standard wells (but not to the blank control well). Mix well. Cover with the adhesive plate sealer provided. Incubate for 60 minutes at 37°C.
Step 7
Remove the plate sealer and wash the plate 5 times with Wash Buffer. Soak wells with 300μl Wash Buffer for 30 seconds to 1 minute for each wash. For automated washing, aspirate or decant each well and wash 5 times with Wash Buffer. 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. Blot the plate onto paper towels or other absorbent material.
Step 8
Add 50μl of Substrate Solution A to each well and then add 50μl of Substrate Solution B to each well. Cover with a new adhesive plate sealer and incubate for 10 minutes at 37°C in the dark.
Step 9
Add 50μl of Stop Solution to each well. The color in the wells should change from blue to yellow immediately. Note: If the color in the wells is green or the color change does not appear uniform, gently tap the plate to ensure thorough mixing.
Step 10
Determine the optical density (O.D. value) of each well within 10 minutes, using a microplate reader set to 450 nm.
Standard Curve - Mouse M6PR (cation independent) ELISA Kit (A312992) - Antibodies.comBild Vergrößern
Figure 1: Standard Curve - Mouse M6PR (cation independent) ELISA Kit (A312992)
Representative standard curve for Mouse M6PR (cation independent) ELISA Kit (A312992).
Hauptmenü Kontakt 0Kasse
Oben