androgen receptor Monoklonaler Antikörper

androgen receptor Monoklonal Antikörper für WB, IHC, IF/ICC, IF-P, Indirect ELISA

Wirt / Isotyp

Maus / IgG2a

Getestete Reaktivität

human, Maus, Ratte

Anwendung

WB, IHC, IF/ICC, IF-P, ChIP, Indirect ELISA

Konjugation

Unkonjugiert

Publikationen(1)

CloneNo.

1F7C12

Kat-Nr. : 66747-1-PBS

Synonyme

androgen receptor,AR, AR, 1F7C12, DHTR, NR3C4



Geprüfte Anwendungen

Veröffentlichte Anwendungen

ChIPSee 1 publications below

Produktinformation

66747-1-PBS bindet in WB, IHC, IF/ICC, IF-P, ChIP, Indirect ELISA androgen receptor und zeigt Reaktivität mit human, Maus, Ratten

Getestete Reaktivität human, Maus, Ratte
In Publikationen genannte Reaktivitäthuman
Wirt / Isotyp Maus / IgG2a
Klonalität Monoklonal
Typ Antikörper
Immunogen androgen receptor fusion protein Ag17291
Vollständiger Name androgen receptor
Berechnetes Molekulargewicht 914 aa, 99 kDa
Beobachtetes Molekulargewicht 110-120 kDa
GenBank-ZugangsnummerBC132975
Gene symbol AR
Gene ID (NCBI) 367
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Protein-A-Reinigung
Lagerungspuffer PBS only
LagerungsbedingungenStore at -80°C. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

AR, also named as DHTR and NR3C4, belongs to the nuclear hormone receptor family and NR3 subfamily. AR is a ligand-activated transcription factors that regulate eukaryotic gene expression and affect cellular proliferation and differentiation in target tissues. Transcription factor activity is modulated by bound coactivator and corepressor proteins. AR is activated, but not phosphorylated, by HIPK3. Defects in AR are the cause of androgen insensitivity syndrome (AIS), previously known as testicular feminization syndrome (TFM), which is an X-linked recessive form of pseudohermaphroditism due end-organ resistance to androgen. Defects in AR are the cause of spinal and bulbar muscular atrophy X-linked type 1 (SMAX1) which also known as Kennedy disease. Defects in AR may play a role in metastatic prostate cancer. Defects in AR are the cause of androgen insensitivity syndrome partial (PAIS) which also known as Reifenstein syndrome. AR exists various isoforms with MW 110-120 kDa and 75-80 kDa. (PMID: 19244107 )

Publikationen

SpeciesApplicationTitle
humanChIP

Sci Rep

Characterization of RNA editing gene APOBEC3C as a candidate tumor suppressor in prostate cancer

Authors - Li-Yang Wang