Full Product Name
ATRX siRNA (Mouse)
Product Synonym Names
HP1BP2; XNP; Transcriptional regulator ATRX; ATP-dependent helicase ATRX; HP1 alpha-interacting protein; HP1-BP38 protein; Heterochromatin protein 2; X-linked nuclear protein
Product Gene Name
ATRX sirna
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q61687
Specificity
ATRX siRNA (Mouse) is a target-specific 19-23 nt siRNA oligo duplexes designed to knock down gene expression.
Purity/Purification
> 97%
Form/Format
Lyophilized powder
Quality Control
Oligonucleotide synthesis is monitored base by base through trityl analysis to ensure appropriate coupling efficiency. The oligo is subsequently purified by affinity-solid phase extraction. The annealed RNA duplex is further analyzed by mass spectrometry to verify the exact composition of the duplex. Each lot is compared to the previous lot by mass spectrometry to ensure maximum lot-to-lot consistency.
Directions for Use
We recommends transfection with 100 nM siRNA 48 to 72 hours prior to cell lysis. Before resuspending, briefly centrifuge the tube to ensure the lyophilized siRNA is at the bottom of the tube. Resuspend the siRNA oligos to an appropriate concentration with DEPC water. For each vial, suitable for 250 transfections in 24 well plate (20 pmol for each well).
Components
We offer pre-designed sets of 3 different target-specific siRNA oligo duplexes of mouse ATRX gene. Each vial contains 5 nmol of lyophilized siRNA. The duplexes can be transfected individually or pooled together to achieve knockdown of the target gene, which is most commonly assessed by qPCR or western blot. Our siRNA oligos are also chemically modified (2'-OMe) at no extra charge for increased stability and enhanced knockdown in vitro and in vivo.
Preparation and Storage
Shipped at 4 degree C. Store at -20 degree C for one year.
Negative Control
siRNA Negative Control (Catalog# MBS8241404) is a non-targeting 21 nt siRNA recommended as a negative control for experiments using targeted siRNA transfection.
Other Notes
Small volumes of ATRX sirna vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
ATRX sirna
siRNA to inhibit ATRX expression using RNA interference
Applications Tested/Suitable for ATRX sirna
RNA Interference (RNAi)
NCBI/Uniprot data below describe general gene information for ATRX. It may not necessarily be applicable to this product.
NCBI Accession #
NP_033556.2
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NCBI GenBank Nucleotide #
NM_009530.2
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UniProt Primary Accession #
Q61687
[Other Products]
UniProt Secondary Accession #
A2ADH4[Other Products]
UniProt Related Accession #
Q61687[Other Products]
Molecular Weight
278,587 Da
NCBI Official Full Name
transcriptional regulator ATRX
NCBI Official Synonym Full Names
alpha thalassemia/mental retardation syndrome X-linked homolog (human)
NCBI Official Symbol
Atrx??[Similar Products]
NCBI Official Synonym Symbols
XH2; Xnp; ATR2; MRXS3; Rad54; Hp1bp2; RAD54L; ZNF-HX; Hp1bp38; AI447451; HP1-BP38; DXHXS6677E; 4833408C14Rik
??[Similar Products]
NCBI Protein Information
transcriptional regulator ATRX
UniProt Protein Name
Transcriptional regulator ATRX
UniProt Synonym Protein Names
ATP-dependent helicase ATRX; HP1 alpha-interacting protein; HP1-BP38 protein; Heterochromatin protein 2; X-linked nuclear protein
Protein Family
Transcriptional regulator
UniProt Gene Name
Atrx??[Similar Products]
UniProt Synonym Gene Names
Hp1bp2; Xnp??[Similar Products]
UniProt Entry Name
ATRX_MOUSE
UniProt Comments for ATRX
ATRX: a global transcriptional regulator. Belongs to the SNF2 family of proteins, many of which modify gene expression via chromatin remodeling activity. Involved in the developmental silencing of imprinted genes in the brain. Contains one PxVxL motif, which is required for interaction with chromoshadow domains. This motif requires additional residues at -7, -6, +4 and +5 relative to the central V which contact the chromoshadow domain. Constitutive mutations in ATRX are associated with brain, facial, and genital abnormalities, and alpha thalassemia. Acquired mutations in ATRX have been observed in preleukemic conditions. Six alternatively spliced human isoforms have been described.
Protein type: EC 3.6.4.12; Helicase; DNA repair, damage; Ubiquitin conjugating system
Cellular Component: nucleoplasm; heterochromatin; nuclear chromosome; chromosome, telomeric region; cytoplasm; chromosome; intracellular; nucleus
Molecular Function: protein binding; DNA binding; zinc ion binding; hydrolase activity; histone binding; metal ion binding; nucleotide binding; chromatin binding; helicase activity; DNA translocase activity; methylated histone residue binding; ATP binding
Biological Process: transcription, DNA-dependent; DNA damage response, signal transduction by p53 class mediator; multicellular organism growth; positive regulation of telomere maintenance; chromatin modification; DNA repair; Sertoli cell development; replication fork processing; chromatin remodeling; nucleosome assembly; regulation of transcription, DNA-dependent; DNA replication-independent nucleosome assembly; post-embryonic forelimb morphogenesis; forebrain development; spermatogenesis; positive regulation of transcription from RNA polymerase II promoter; response to DNA damage stimulus
Research Articles on ATRX
1. Using X chromosome inactivation as a model, study applied an unbiased proteomics approach to isolate Xist and PRC2 regulators and identified ATRX; ATRX functions as a high-affinity RNA-binding protein that directly interacts with RepA/Xist RNA to promote loading of PRC2 in vivo. Without ATRX, PRC2 cannot load onto Xist RNA nor spread in cis along the X chromosome.
Precautions
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Disclaimer
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