Anticorps Monoclonal anti-androgen receptor

androgen receptor Monoclonal Antibody for WB, IHC, IF/ICC, IF-P, Indirect ELISA

Hôte / Isotype

Mouse / IgG2a

Réactivité testée

Humain, rat, souris

Applications

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

Conjugaison

Non conjugué

Publications(1)

CloneNo.

1F7C12

N° de cat : 66747-1-PBS

Synonymes

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



Applications publiées

ChIPSee 1 publications below

Informations sur le produit

66747-1-PBS cible androgen receptor dans les applications de WB, IHC, IF/ICC, IF-P, ChIP, Indirect ELISA et montre une réactivité avec des échantillons Humain, rat, souris

Réactivité Humain, rat, souris
Réactivité citéeHumain
Hôte / Isotype Mouse / IgG2a
Clonalité Monoclonal
Type Anticorps
Immunogène androgen receptor Protéine recombinante Ag17291
Nom complet androgen receptor
Masse moléculaire calculée 914 aa, 99 kDa
Poids moléculaire observé 110-120 kDa
Numéro d’acquisition GenBankBC132975
Symbole du gène AR
Identification du gène (NCBI) 367
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par protéine A
Tampon de stockage PBS only
Conditions de stockageStore at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

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 )

Publications

SpeciesApplicationTitle
humanChIP

Sci Rep

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

Authors - Li-Yang Wang
{{ptg:RelatedPrimaryAntibodies}}