Anti-Human CD28 PE-Cyanine7

Also known as: T44

Clone: CD28.2

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

SKU# 25-0289

Cat. No. Size
25-0289-41 25 tests
25-0289-42 100 tests
Please inquire about custom configurations or bulk packaging.

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Data for Anti-Human CD28 PE-Cy7.

Staining of normal human peripheral blood cells with Anti-Human CD19 FITC (cat. 11-0199) and Mouse...View More

  • Data for Anti-Human CD28 PE-Cy7.
Description

Description: The CD28.2 monoclonal antibody reacts with the human CD28 molecule, a 44 kDa homodimer expressed by thymocytes, mature T cells and plasma cells. CD28 is a ligand for CD80 (B7-1) and CD86 (B7-2) and is a potent co-stimulator of T cells. Signaling through CD28 augments IL-2 and IL-2 receptor expression as well as cytotoxicity of CD3-activated T cells.

Details
Host Mouse
Isotype IgG1, kappa
Reactivity Human
Conjugate PE-Cyanine7
Laser Blue Laser, Green Laser, Yellow-Green Laser
Emit 775 nm
Excite 488 - 561 nm
Legal FOR NON-COMMERCIAL RESEARCH USE ONLY. NOT FOR THERAPEUTIC OR IN VIVO APPLICATIONS. OTHER USE NEEDS LICENSE FROM GE HEALTHCARE BIO-SCIENCES CORP. UNDER U.S. PATENT FOR NON-COMMERCIAL RESEARCH USE ONLY. NOT FOR THERAPEUTIC OR IN VIVO APPLICATIONS. OTHER USE NEEDS LICENSE FROM GE HEALTHCARE BIO-SCIENCES CORP. UNDER U.S. PATENT # 5,268,486, 5,569,587 AND 5,627,027 AND FOREIGN EQUIVALENTS AND PENDING APPLICATIONS. THIS MATERIAL IS SUBJECT TO PROPRIETARY RIGHTS OF GE HEALTHCARE BIO-SCIENCES CORP. AND CARNEGIE MELLON UNIVERSITY AND MADE AND SOLD UNDER LICENSE FROM GE HEALTHCARE BIO-SCIENCES CORP. THIS PRODUCT IS LICENSED FOR SALE ONLY FOR RESEARCH. IT IS NOT LICENSED FOR ANY OTHER USE. THERE IS NO IMPLIED LICENSE HEREUNDER FOR ANY COMMERCIAL USE. COMMERCIAL USE shall include: 1. sale, lease, license or other transfer of the material or any material derived or produced from it; 2. sale, lease, license or other grant of rights to use this Material or any material derived or produced from it; 3. use of this material to perform services for a fee for third parties. IF YOU REQUIRE A COMMERCIAL LICENSE TO USE THIS MATERIAL AND DO NOT HAVE ONE, RETURN THIS MATERIAL, UNOPENED TO EBIOSCIENCE, INC. 10255 SCIENCE CENTER DRIVE, SAN DIEGO, CALIFORNIA 92121 USA AND ANY MONEY PAID FOR THE MATERIAL WILL BE REFUNDED.
Reported Applications Flow Cytometric Analysis
Documentation
TDS Link Download TDS
Additional Formats
Cat. No. Name Excite Emit Application Reg.
14-0289 Anti-Human CD28 Purified FC, IHC, FA, IP RUO
12-0289 Anti-Human CD28 PE 488 - 561 nm 575 nm FC RUO
16-0289 Anti-Human CD28 Functional Grade Purified FC, FA RUO
11-0289 Anti-Human CD28 FITC 488 nm 518 nm FC RUO
17-0289 Anti-Human CD28 APC 633 - 647 nm 660 nm FC RUO
48-0289 Anti-Human CD28 eFluor® 450 405 nm 450 nm FC RUO
47-0289 Anti-Human CD28 APC-eFluor® 780 633 - 647 nm 780 nm FC RUO
45-0289 Anti-Human CD28 PerCP-Cyanine5.5 488 nm FC RUO
13-0289 Anti-Human CD28 Biotin FC RUO
Related Products
Cat. No. Name Excite Emit Application Reg.
11-0199 Anti-Human CD19 FITC 488 nm 518 nm FC RUO
25-4714 Mouse IgG1 K Isotype Control PE-Cyanine7 488 - 561 nm 775 nm FC RUO
References

References: Karlsson I, Malleret B, Brochard P, Delache B, Calvo J, Le Grand R, Vaslin B. FoxP3+ CD25+ CD8+ T-cell induction during primary simian immunodeficiency virus infection in cynomolgus macaques correlates with low CD4+ T-cell activation and high viral load. J Virol. 2007 Dec;81(24):13444-55 (CD28.1, NHP crossreactivity)

Battifora M, Pesce G, Paolieri F, Fiorino N, Giordano C, Riccio AM, Torre G, Olive D, Bagnasco M. B7.1 costimulatory molecule is expressed on thyroid follicular cells in Hashimoto's thyroiditis, but not in Graves' disease. J Clin Endocrinol Metab. 1998 Nov;83(11):4130-9. (CD28.1, IHC frozen)

Nunès J, Klasen S, Ragueneau M, Pavon C, Couez D, Mawas C, Bagnasco M, Olive D. CD28 mAbs with distinct binding properties differ in their ability to induce T cell activation: analysis of early and late activation events. Int Immunol. 1993 Mar;5(3):311-5.

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


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