Human AR Knockdown Cell Lysate

Cat.No. : AR-047HKCL
Product Overview : WB-validated AR Knockdown HeLa Cell Lysate
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  • Gene Information
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Species : Human
Source : HeLa
Tag : Non
Description : 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.
Form : Cell-Tissue Lysis buffer
Molecular Mass : 99 kDa
Notes : Instruction of use: This knockdown cell lysate should be paired with wild-type HeLa cell lysate for use. For Western blotting, we recommend running wild-type and knockdown lysates on the same gel, and loading each well with equal volume and equal amount of total proteins.
Storage : Store at -20 centigrade for two years.
Concentration : Lot-specific
Shipping : Blue Ice
Components : 1 vial of 100 μg WT HeLa cell lysate 1 vial of 100 μg AR KD HeLa cell lysate
Protein Families : Druggable Genome, Nuclear Hormone Receptor, Transcription Factors
Protein Pathways : Oocyte meiosis, Pathways in cancer, Prostate cancer
Lysate QC : RT-qPCR; Western Blotting (WB)
Gene Name AR androgen receptor [ Homo sapiens (human) ]
Official Symbol AR
Synonyms AR; androgen receptor; DHTR, dihydrotestosterone receptor, SBMA, spinal and bulbar muscular atrophy; AIS; HUMARA; Kennedy disease; NR3C4; SMAX1; testicular feminization; dihydrotestosterone receptor; androgen nuclear receptor variant 2; nuclear receptor subfamily 3 group C member 4; KD; TFM; DHTR; SBMA; HYSP1;
Gene ID 367
mRNA Refseq NM_000044
Protein Refseq NP_000035
MIM 313700
UniProt ID P10275

Not For Human Consumption!

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