Anti-Human CD42b PE

Clone: HIP1

RUO: For Research Use Only. Not for use in diagnostic procedures.

SKU# 12-0429

Cat. No. Size
12-0429-42 100 tests
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Data for Anti-Human CD42b PE.

Staining of human platelets with Anti-Human CD41a FITC (cat. 11-0419) and Mouse IgG1 K Isotype...View More

  • Data for Anti-Human CD42b PE.
Description

Description: The HIP1 monoclonal antibody reacts with the human CD42b molecule, a 135 kDa transmembrane protein also known as platelet gpIb.

Details
Host Mouse
Isotype IgG1, kappa
Reactivity Human
Conjugate PE
Laser Blue Laser, Green Laser, Yellow-Green Laser
Excite 488 - 561 nm
Reported Applications Flow Cytometric Analysis
Documentation
TDS Link Download TDS
Additional Formats
Cat. No. Name Excite Emit Application Reg.
16-0429 Anti-Human CD42b Functional Grade Purified FC, FA RUO
17-0429 Anti-Human CD42b APC 633 - 647 nm 660 nm FC RUO
14-0429 Anti-Human CD42b Purified FC, IHC, FA, WB RUO
11-0429 Anti-Human CD42b FITC 488 nm FC RUO
Related Products
Cat. No. Name Excite Emit Application Reg.
11-0419 Anti-Human CD41a FITC 488 nm FC RUO
12-4714 Mouse IgG1 K Isotype Control PE 488 - 561 nm 575 nm FC RUO
References

References: Takahashi R, Sekine N, Nakatake T. Influence of Monoclonal Antiplatelet Glycoprotein Antibodies on In Vitro Human Megakaryocyte Colony Formation and Proplatelet Formation. Blood. 1999 Mar 15;93(6):1951-8. (FA, PubMed)

Gohda F, Uchiumi H, Handa H, Matsushima T, Tsukamoto N, Morita K, Amagai H, Murakami M, Murakami H, Nojima Y, Karasawa M. Identification of inherited macrothrombocytopenias based on mean platelet volume among patients diagnosed with idiopathic thrombocytopenia. Thromb Res. 2007;119(6):741-6. (FC, PubMed)

George NP, Wei Q, Shin PK, Konstantopoulos K, Ross JM. Staphylcococcus aureus adhesion via Spa, ClfA, and SdrCDE to immobilized platelets demonstrates shear-dependent behavior. Arterioscler Thromb Vasc Biol. 2006 Oct;26(10):2394-400. (FA, PubMed)

Schlossman, S., L. Bloumsell, et al. eds (1995). Leucocyte Typing V: White Cell Differentiation Antigens. Oxford University Press. New York.


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