AR (Acetyl Lys633) rabbit pAb

AR (Acetyl Lys633) rabbit pAb

AO-06-ES8620-100

AR (Acetyl Lys633) rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES8620
Product nameAR (Acetyl Lys633) rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameAndrogen receptor (Dihydrotestosterone receptor) (Nuclear receptor subfamily 3 group C member 4)
Size100μL
Unit price ($)248
Human gene ID367
Human Swiss-ProtP10275
SourceRabbit
IsotypeIgG
TargetAndrogen Receptor
Fields>>Oocyte meiosis;>>Pathways in cancer;>>Chemical carcinogenesis - receptor activation;>>Prostate cancer
Gene nameAR DHTR NR3C4
Protein nameAndrogen receptor (Dihydrotestosterone receptor) (Nuclear receptor subfamily 3 group C member 4)
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtP19091
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-ProtP15207
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthetic Acetyl peptide from human protein at AA range: 633
SpecificityThis antibody detects endogenous levels of AR at Human:K633;Mouse:K613;Rat:K616, It doesn't reacte with total protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000, ELISA 1:10000-20000
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)100kD
BackgroundThe androgen receptor gene is more than 90 kb long and codes for a protein that has 3 major functional domains: the N-terminal domain, DNA-binding domain, and androgen-binding domain. The protein functions as a steroid-hormone activated transcription factor. Upon binding the hormone ligand, the receptor dissociates from accessory proteins, translocates into the nucleus, dimerizes, and then stimulates transcription of androgen responsive genes. This gene contains 2 polymorphic trinucleotide repeat segments that encode polyglutamine and polyglycine tracts in the N-terminal transactivation domain of its protein. Expansion of the polyglutamine tract from the normal 9-34 repeats to the pathogenic 38-62 repeats causes spinal bulbar muscular atrophy (Kennedy disease). Mutations in this gene are also associated with complete androgen insensitivity (CAIS). Two alternatively spliced variants encoding distinct isoform
Functiondisease:Defects in AR are the cause of androgen insensitivity syndrome (AIS) [MIM:300068]; previously known as testicular feminization syndrome (TFM). AIS is an X-linked recessive form of pseudohermaphroditism due end-organ resistance to androgen. Affected males have female external genitalia, female breast development, blind vagina, absent uterus and female adnexa, and abdominal or inguinal testes, despite a normal 46,XY karyotype.,disease:Defects in AR are the cause of androgen insensitivity syndrome partial (PAIS) [MIM:312300]; also known as Reifenstein syndrome. PAIS is characterized by hypospadias, hypogonadism, gynecomastia, genital ambiguity, normal XY karyotype, and a pedigree pattern consistent with X-linked recessive inheritance. Some patients present azoospermia or severe oligospermia without other clinical manifestations.,disease:Defects in AR are the cause of spinal and bulb
Subcellular locationNucleus . Cytoplasm . Detected at the promoter of target genes (PubMed:25091737). Predominantly cytoplasmic in unligated form but translocates to the nucleus upon ligand-binding. Can also translocate to the nucleus in unligated form in the presence of RACK1. .
Expression[Isoform 2]: Mainly expressed in heart and skeletal muscle. ; [Isoform 3]: Expressed in basal and stromal cells of the prostate (at protein level).

Additional Images

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Western blot analysis of mouse-lung lysate, antibody was diluted at 500. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
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: AO-06-ES8620-100
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Hurry! only 10 items left in stock.

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