Anti-Pan-Cytokeratin (AE1/AE3) Alexa Fluor® 488

Also known as: keratin, basic, acidic

Clone: AE1/AE3

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

SKU# 53-9003

Cat. No. Size
53-9003-80 25 ug
53-9003-82 100 ug
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Data for Anti-Pan-Cytokeratin (AE1/AE3) Alexa Fluor® 488.

Immunofluorescent microscopy of fixed and permeabilized MCF-7 cells using 1 ug/ml of Mouse IgG1...View More

  • Data for Anti-Pan-Cytokeratin (AE1/AE3) Alexa Fluor® 488.
Description

Description: The monoclonal antibodies AE1 and AE3 recognize many of the acidic and basic cytokeratin family members. Cytokeratins are intermediate filament proteins comprising one component of the cytoskeleton. There are two large families of cytokeratins, acidic and basic, but all contain the same basic domains (i.e. an α-helical core with an N- and C-terminal domain). The proteins are expressed in epithelial cells, but are developmentally regulated. Many tumors also express these proteins and their expression can help identify the origin of a neoplasm.

The AE3 monoclonal antibody recognizes the 65 to 67 triplet, 64, 59, 58, 56, and 52kD proteins also known as cytokeratin 1, 2, 3, 4, 5, 6, 7) while the AE1 antibody recognizes 56.5, 50, 50’, 48, and 40 kDa proteins (also known as CK10, 14, 15, 16 and 19). These antibodies can be used on a wide array of tissue samples from mouse, human, rat, primates (cynomolgus and rhesus), dog, cat, rabbit, and chicken.

Details
Host Mouse
Isotype IgG1
Reactivity Canine, Human, Monkey, Mouse, Rabbit, Rhesus
Conjugate Alexa Fluor 488
Laser Blue Laser
Emit 519 nm
Excite 488 nm
Legal Alexa Fluor® and Pacific Blue® are registered trademarks of and licensed under patents assigned to Molecular Probes, Inc. for research use only. This product is subject to an agreement between Molecular Probes, Inc. and eBioscience, and the manufacture, use, sale or import of this product may be subject to one or more U.S. patents, pending applications and corresponding foreign equivalents, owned by Molecular Probes, Inc. (a wholly owned subsidiary of Invitrogen Corp). The purchase of this product conveys to the buyer the non-transferable right to use the purchased amount of the product for life science research or as an ASR. The buyer cannot use this product for manufacturing or for any other screening (specifically including use in combination with microarrays or High Content Screening) or testing purpose, other than as an ASR. For information on purchasing a license to this product for purposes other than life science research or use as an ASR, contact Molecular Probes, Inc.
Reported Applications Immunohistochemical Staining of Frozen Tissue Sections, Immunocytochemistry
Documentation
TDS Link Download TDS
Additional Formats
Cat. No. Name Excite Emit Application Reg.
41-9003 Anti-Pan Cytokeratin (AE1/AE3) eFluor® 570 555 nm 570 nm ICC RUO
42-9003 Anti-Pan Cytokeratin (AE1/AE3) eFluor® 615 595 nm 615 nm ICC, IHC RUO
Related Products
Cat. No. Name Excite Emit Application Reg.
14-9000 Anti-Basic Cytokeratin Purified IHC, WB RUO
14-9001 Anti-Acidic Cytokeratin Purified IHC, WB RUO
53-4714 Mouse IgG1 K Isotype Control Alexa Fluor® 488 488 nm 519 nm FC, ICC, IHC RUO
References

References: Sato T, Maeda H, Suzuki A, Shibuya H, Sakata A, Shirai W. Endometrial stromal sarcoma with smooth muscle and glandular differentiation of the feline uterus. Vet Pathol. 2007 May;44(3):379-82. (AE1/AE3, IHC, feline)

Chen SS, Revoltella RP, Papini S, Michelini M, Fitzgerald W, Zimmerberg J, Margolis L. Multilineage differentiation of rhesus monkey embryonic stem cells in three-dimensional culture systems. Stem Cells. 2003;21(3):281-95.(AE1/AE3, IHC, rhesus)

Woodcock-Mitchell J, Eichner R, Nelson WG, Sun TT. Immunolocalization of keratin polypeptides in human epidermis using monoclonal antibodies. J Cell Biol. 1982 Nov;95(2 Pt 1):580-8. (AE1/AE3, WB, IHC, PubMed)

Tseng SC, Jarvinen MJ, Nelson WG, Huang JW, Woodcock-Mitchell J, Sun TT. Correlation of specific keratins with different types of epithelial differentiation: monoclonal antibody studies. Cell. 1982 Sep;30(2):361-72.


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