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product summary
company name :
US Biological
product type :
antibody
product name :
NF-kB p65, phosphorylated (Ser536) (Nuclear Factor kB) (AlexaFluor®488)
catalog :
N2303-05A
quantity :
100 ul
clonality :
monoclonal
host :
domestic rabbit
conjugate :
AF488
antigen modification :
phosphorylated
clone name :
5i125(93H1)
reactivity :
human
product information
Catalog Number :
N2303-05A
Product wo Prefix :
NF-kB p65, phosphorylated (Ser536) (Nuclear Factor kB) (AlexaFluor®488)
Host :
rabbit
Product Type :
Mab
Conjugate :
Alexa Fluor®488
Antigen Modification :
Phosphorylated
Category :
Antibodies
Size1 :
100 ul
Clone # USB :
5i125(93H1)
Isotype :
IgG
Desc1 :
Transcription factors of the nuclear factor kB (NF-kB)/Rel family play a pivotal role in inflammatory and immune responses. There are five family members in mammals; RelA, c-Rel, RelB, NF-kB1 p105/p50), and NF-kB2 (p100/p52). p105 and p100 are proteolytically processed by the proteasome to produce p50 and p52, respectively. The p50 and p52 products form dimeric complexes with Rel proteins, which are then able to bind DNA and regulate transcription. In unstimulated cells, NF-kB is sequestered in the cytoplasm by its inhibitory proteins, the IkBs. NF-kBactivating agents can induce the phosphorylation of IkBs, which targets them for rapid degradation through a ubiquitin-proteasome pathway, releasing NF-kB to enter the nucleus and regulate gene expression. Processing of NF-kB2 is regulated by IKK1 (IKK-a), which triggers the phosphorylation and processing to p52, which can then undergo nuclear translocation.
Applications:
Suitable for use in Flow Cytometry. Other applications not tested.
Recommended Dilution:
Flow Cytometry: 1:10. Add 10ul of the conjugated antibody to 500K cells in 90ul PBS/0.5% BSA.
Optimal dilutions to be determined by the researcher.
Storage and Stability:
Store at 4° C before opening. DO NOT FREEZE. This product is stable at 4° C as an undiluted liquid. Dilute only prior to immediate use. Freezing Alexa Fluor®488 conjugates will result in a substantial loss of enzymatic activity.
Calc Crossreactivity :
Hm Hu Mk Mo Po Rt
Immunogen :
Synthetic phosphopeptide corresponding to residues surrounding Ser536 of human NF-kB p65. Species sequence homology: canine
Specificity :
Detects human NF-kB p65 only when phosphorylated at serine 536. Does not cross-react with the p50 subunit or other related proteins. Species Crossreactivity: human, mouse, rat, hamster, monkey and porcine
Purity :
Purified by immunoaffinity chromatography
Form :
Supplied as a liquid in PBS, pH 7.2, 2mg/ml BSA, 0.09% sodium azide. Labeled with AelxaFluor 488.
Concentration :
Not determined
Desc2 :
Product Type: Mab
Isotype: IgG
Clone No: 5i125(93H1)
Host: rabbit
Source: human
Concentration: Not determined
Form: Supplied as a liquid in PBS, pH 7.2, 2mg/ml BSA, 0.09% sodium azide. Labeled with AelxaFluor 488.
Purity: Purified by immunoaffinity chromatography.
Immunogen: Synthetic phosphopeptide corresponding to residues surrounding Ser536 of human NF-kB p65. Species sequence homology: canine
Specificity: Detects human NF-kB p65 only when phosphorylated at serine 536. Does not cross-react with the p50 subunit or other related proteins. Species Crossreactivity: human, mouse, rat, hamster, monkey and porcine
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Calc Applications Abbrev :
FC
Storage Temperature :
4°C Do not freeze
Reference :
1. Baeuerle, P.A. and Henkel, T. (1994) Annu. Rev. Immunol. 12: 141–179. 2 Baeuerle, P.A. and Baltimore, D. (1996) Cell 87: 13–20. (3) Haskill, S. et al. (1991) Cell 65: 1281–1289. (4) Thompson, J.E. et al. (1995) Cell 80: 573–582. (5) Whiteside, S.T. et al. (1997) EMBO J. 16: 1413–1426. (6) Traenckner, E.B. et al. (1995) EMBO J. 14: 2876–2883. (7) Scherer, D.C. et al. (1995) Proc. Natl. Acad. Sci. USA 92;11259–11263. (8) Chen, Z.J. et al. (1996) Cell 8:, 853–862. (9) Senftleben, U. et al. (2001) Science 293: 1495–1499. (10) Coope, H. J. et al. (2002) EMBO J. 21, 5375–5385. (11) Xiao, G. et al. (2001) Mol. Cell 7, 401–409. 1. Spieker-Polet H, et al. Proc Natl Acad Sci. 1995 Sep 26;92(20):9348-52. 2. Liguori MJ, et al. Hybridoma. 2001 Jun; 20(3):189-98. 3. G.Cano1, F. Milanezi2, D. Leitao2,3, S. Ricardo2, M.J. Brito1, F. C. Schmitt2-3 1Garcia da Orta Hospital, Almada, Portugal,2 Inst. Molec. Pathology and Immunology of Porto University, Portugal,3 Medical Faculty of Porto university, Portugal Diagn Cytopathol, 2003 Oct; 29(4): 207 -11. 4. L.K. Diaz* and N.Sneige *Department of Pathology,Northwestern University, Chicago,+ Department of Pathology, University of Texas, Huston, Adv Anat Pathol,2005; 12(1), 10-19. 5. Z. Huang1, W. Zhu2, G. Szekeres3, H. Xia1 1Spring Bioscience Corp, Fremont,CA, 2 Epitomics Inc, Burlingame,CA, , 4Histopathology Ltd, Hungary, Appl Immunohistochem Mol Morphol. 2005; 13 (1): 91-95 6. S. Rossi1, E. Orvieto1, S.Chinellato1, A. Furlanetto1, L.Laurino1, F. Facchetti2, AP Dei Tos 2 1Department of Pathology, 2Treviso, Italy; *Brescia, University School of Medicine, Brescia, Italy., Abstract presented at USCAP 2004. Modern Pathology 2004; 17 (suppl 1): 361A 7. M. Blechner, E. Ballesteros, D. Mandich, D. Stevens, R. Cartun, Hartford Hospital, Hartford, CT. Abstract presented at USCAP 2004. Modern Pathology 2004; 17 (suppl 1): 241A 8. W. Cheuk, K.O.Y. Wong, C.S.C. Wong and J.K.C. Chan, Department of Pathology, Queen Elizabeth Hospital, Hong Kong, Am J Surg Path, 2004; 28 (6): 801-807. 9. G.B. Budd, E. Tso, B. Yoder, T. Choueiri, P. Elson, S. Tarr, M. Skacel, R. Tubbs, A. Dawson, D. Hicks, Cleveland Clinic Foundation, Cleveland, OH, Abstract presented at ASCO Annual meeting, June 2004, New Orleans 10. S. M. Tarr, S. Short, K. Hansen, T. Morken, H. Xia, E. Downs-Kelly, R. R. Tubbs, D. G. Hicks, Department of Pathology and Laboratory Medicine. The Cleveland Clinic Foundation, Cleveland, Ohio. Lab Vision Corp., Fremont, Ca., Spring Bioscience Corp, Fremont ,CA, Abstract presented at Association for Molecular Pathology meeting, Los Angeles, 2004 11. A.M. Gown, T.S. Barry, P. Kandalaft, L.C. Goldstein, C.C. Tse and D.O. Treaba, Clinical Research Division , PhenoPath Laboratories and IMPRIS, Seattle, WA, Abstract presented at USCAP 2005. Modern Pathology 2005; 18, suppl.1,pag 35A 12. D.O. Treaba, A.W. Hing, L.C. Goldstein, T.S. Barry, P. Kandalaft, C.B. Gilks, T.O. Nielsen and A.M. Gown, Clinical Research Division , PhenoPath Laboratories and IMPRIS, Seattle, WA, USA Genetic Pathology Evaluation Centre, University of British Columbia, Vancouver, BC, Canada, Abstract presented at USCAP 2005. Modern Pathology 2005; 18, suppl.1,pag 53A 13. S. Rossi1, L. Laurino1, A. Furlanetto1, S.Chinellato1, E. Orvieto1, F. Canal1, F. Facchetti2, A.P. Dei Tos1 1 Depart. Pathology, Hospital of Treviso, Italy, 2 Brescia University School of Medicine, Brescia, Italy, Am J Clin Pathol, 2005, Aug;124(2):295-302
Picture 1 File Name :
https://usbio-images.r.worldssl.net/prodimages/43/N2303-05A_1.jpg
company information
US Biological
4 Technology Way
Salem, MA01970
Salem, MA01970
service@usbio.net
https://www.usbio.net800-520-3011
headquarters: USA
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