KD-Validated Androgen Receptor Recombinant Rabbit Monoclonal Antibody

KD-Validated Androgen Receptor Recombinant Rabbit Monoclonal Antibody

Cat. No.: KVAb01633
Size:20μL Price:$118
Size:50μL Price:$218
Size:100μL Price:$318
Application:WB,ICC,IHC-P

Reactivity:Human,Mouse
Conjugate:Unconjugated
Gene Name:AR
Category: KO&KD Validated Antibodies Tags: , , , , , , , ,

Summary

Production Name

KD-Validated Androgen Receptor Recombinant Rabbit Monoclonal Antibody

Description

KD-Validated antibody

Host

Rabbit

Application

WB,ICC,IHC-P

Reactivity

Human,Mouse

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Rabbit IgG

Clonality

Rabbit mAb

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.

Purification

Affinity purification

 

Immunogen

Gene Name

AR

Alternative Names

AR; Androgen Receptor; NR3C4; Dihydrotestosterone Receptor; HUMARA; SMAX1; DHTR; AIS; Nuclear Receptor Subfamily 3 Group C Member; SBMA; Spinal And Bulbar Muscular Atrophy; Testicular; Feminization; Kennedy Disease; HYSP1; AR8; TFM; KD

Gene ID

367

SwissProt ID

P10275

 

Application

Dilution Ratio

WB 1:1,000-1:5,000; ICC 1:100-1:1,000; IHC-P 1:100-1:200

Molecular Weight

Calculated MW: 99.2kDa

 

Background

The 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 (SBMA, also known as Kennedy's disease). Mutations in this gene are also associated with complete androgen insensitivity (CAIS). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2017]

 

Research Area

Signal Transduction

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