mAb anti-Human PSA (CHYH1, Capture) MO-T40081A from Anogen | Biocompare.com

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mAb anti-Human PSA (CHYH1, Capture)

The mAb anti-Human PSA (CHYH1, Capture) Antibody from Anogen is a Mouse Monoclonal antibody. This antibody recognizes Human antigen. The mAb anti-Human PSA (CHYH1, Capture) Antibody has been validated for the following applications: EIA, Immunoassay, ELISA, Immunocytochemistry, and Western Blot.

Product Specs
ItemmAb anti-Human PSA (CHYH1, Capture)
CompanyAnogen
Price Pricing Info Supplier Page View Company Product Page
Catalog NumberMO-T40081A
Quantity0.5 mg
ApplicationsELISA, Western Blot, Immunocytochemistry
ConcentrationDouble distilled water is recommended to reconstitute the antibody
Conjugate/TagUnconjugated
FormatLyophilized from a solution in 0.01M PBS, pH 7.0
PurityProtein G affinity purified
ReactivityHuman
TargetProstate Specific Antigen (PSA)
IsotypeIgG1 kappa
CloneCHYH1
HostMouse
Antibody TypePrimary
ImmunogenHuman Prostate Specific antigen (PSA)
ClonalityMonoclonal
Research AreaTumor Research

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Anogen

Anogen

Anogen 2355 Derry Road East, Unit 23

Mississauga, Ontario

Canada

Phone: 1-877-755-8324

Email: info@anogen.ca

Company Profile

Website: anogen.net

(1) A nanowire-based label-free immunosensor: direct incorporation of a PSA antibody in electropolymerized polypyrroleBiosensors & bioelectronicsJuly 15, 2014Moon JM, Kim YH, Cho Y.

(2) Ultrasensitive Immunosensor for Cancer Biomarker Proteins Using Gold Nanoparticle Film Electrodes and Multienzyme-Particle AmplificationACS NanoMarch 24, 2009Vigneshwaran Mani, Bhaskara V. Chikkaveeraiah, Vyomesh Patel, J. Silvio Gutkind, James F. Rusling

(3) Characterization of multienzyme-antibody-carbon nanotube bioconjugates for immunosensorsJournal of nanoscience and nanotechnologyJanuary 1, 2009Jensen GC, Yu X, Gong JD, Munge B, Bhirde A, Kim SN, Papadimitrakopoulos F, Rusling JF.

(4) Quantum-dot-based electrochemical immunoassay for high-throughput screening of the prostate-specific antigenSmall (Weinheim an der Bergstrasse, Germany)January 1, 2008Wang J, Liu G, Wu H, Lin Y.

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