androgen receptor Monoklonaler Antikörper

androgen receptor Monoklonal Antikörper für IF, IHC, WB, ELISA

Wirt / Isotyp

Maus / IgG2a

Getestete Reaktivität

human, Maus, Ratte

Anwendung

WB, IP, IHC, IF, ELISA

Konjugation

Unkonjugiert

CloneNo.

1F7C12

Kat-Nr. : 66747-1-Ig

Synonyme

AIS, androgen receptor, AR, DHTR, Dihydrotestosterone receptor, HUMARA, HYSP1, KD, NR3C4, SBMA, SMAX1, TFM



Geprüfte Anwendungen

Erfolgreiche Detektion in WBLNCaP-Zellen, humanes Hodengewebe, NCCIT-Zellen
Erfolgreiche Detektion in IHChumanes Prostatakarzinomgewebe, Maushodengewebe, Rattenhodengewebe
Hinweis: Antigendemaskierung mit TE-Puffer pH 9,0 empfohlen. (*) Wahlweise kann die Antigendemaskierung auch mit Citratpuffer pH 6,0 erfolgen.
Erfolgreiche Detektion in IFhumanes Prostatakarzinomgewebe, LNCaP-Zellen

Empfohlene Verdünnung

AnwendungVerdünnung
Western Blot (WB)WB : 1:600-1:3000
Immunhistochemie (IHC)IHC : 1:5000-1:20000
Immunfluoreszenz (IF)IF : 1:200-1:800
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, check data in validation data gallery

Produktinformation

66747-1-Ig bindet in WB, IP, IHC, IF, ELISA androgen receptor und zeigt Reaktivität mit human, Maus, Ratten

Getestete Reaktivität human, Maus, Ratte
In Publikationen genannte Reaktivitäthuman, Maus, Ratte
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 mit 0.02% Natriumazid und 50% Glycerin pH 7.3.
LagerungsbedingungenBei -20°C lagern. Nach dem Versand ein Jahr lang stabil Aliquotieren ist bei -20oC Lagerung nicht notwendig. 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 )

Protokolle

Produktspezifische Protokolle
WB protocol for androgen receptor antibody 66747-1-IgProtokoll herunterladen
IHC protocol for androgen receptor antibody 66747-1-IgProtokoll herunterladen
IF protocol for androgen receptor antibody 66747-1-IgProtokoll herunterladen
Standard-Protokolle
Klicken Sie hier, um unsere Standardprotokolle anzuzeigen

Publikationen

SpeciesApplicationTitle
ratIHC

Development

Human prostate organoid generation and the identification of prostate development drivers using inductive rodent tissues

Authors - Parmveer Singh
ratWB

Chin J Nat Med

Eucommia lignans alleviate the progression of diabetic nephropathy through mediating the AR/Nrf2/HO-1/AMPK axis in vivo and in vitro

Authors - Qi Huang
human,mouseWB,IF,IP

iScience

WTAP boosts lipid oxidation and induces diabetic cardiac fibrosis by enhancing AR methylation

Authors - Kai Song
humanWB,IF

Gynecol Endocrinol

N6-methyladenosine demethylase FTO related to hyperandrogenism in PCOS via AKT pathway

Authors - Yuan-Xue Jing