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Antigenic Specificity | AR Phospho pY267, internal |
Clone | polyclonal |
Host Species | Rabbit |
Reactive Species | human |
Isotype | n/a |
Format | immunoaffinity purified |
Size | 50 µg |
Concentration | 1.1 mg/mL |
Applications | ELISA, Western Blot. Anti-Androgen Receptor antibody is useful for ELISA, Immunohistochemistry, and Western Blot. Specific conditions for reactivity should be optimized by the end user. Expect a band approximately ~99kDa corresponding to the appropriate cell lysate or extract. |
Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
Description | Anti-Androgen Receptor pY267 was affinity purified from monospecific antiserum by immunoaffinity chromatography. A BLAST analysis was used to suggest cross-reactivity with human and chimpanzee based on 100% sequence homology. Cross-reactivity with Androgen Receptor pY267 from other sources has not been determined. |
Immunogen | Anti-Androgen Receptor pY267 affinity purified antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to the internal region of human ANDR protein. |
Other Names | rabbit Anti-Androgen Receptor pY267 antibody, Dihydrotestosterone receptor, DHTR, NR3C4, rabbit Anti-AR pY267 Antibody |
Gene, Accession # | AR, UniProt: P10275 |
Catalog # | 600-401-J95 |
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Order / More Info | AR Phospho pY267, internal Antibody from ROCKLAND IMMUNOCHEMICALS INC. |
Product Specific References | N. Mahajan, Y. Liu, S. Majumder, M. Warren, C. Parker, J. Mohler, H. Earp, and Y. Whang. (2007) Activated Cdc42-associated kinase Ack1 promotes prostate cancer progression via androgen receptor tyrosine phosphorylation. PNAS vol. 104 no. 20 8438-8443, doi: 10.1073/pnas.0700420104.Liu Y, Karaca M, Zhang Z, Gioeli D, Earp HS, Whang YE. (2010) Dasatinib inhibits site-specific tyrosine phosphorylation of androgen receptor by Ack1 and Src kinases. Oncogene. Jun 3;29(22):3208-16. doi: 10.1038/onc.2010.103. Epub Apr 12. |
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