Full Product Name
EDN3 siRNA (Mouse)
Product Synonym Names
Endothelin-3; ET-3; Preproendothelin-3; PPET3
Product Gene Name
EDN3 sirna
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for P48299
Specificity
EDN3 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 EDN3 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 EDN3 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
EDN3 sirna
siRNA to inhibit EDN3 expression using RNA interference
Applications Tested/Suitable for EDN3 sirna
RNA Interference (RNAi)
NCBI/Uniprot data below describe general gene information for EDN3. It may not necessarily be applicable to this product.
NCBI Accession #
NP_031929.1
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NCBI GenBank Nucleotide #
NM_007903.4
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UniProt Primary Accession #
P48299
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UniProt Secondary Accession #
Q543L0[Other Products]
UniProt Related Accession #
P48299[Other Products]
Molecular Weight
23,322 Da
NCBI Official Full Name
endothelin-3 preproprotein
NCBI Official Synonym Full Names
endothelin 3
NCBI Official Symbol
Edn3??[Similar Products]
NCBI Official Synonym Symbols
ls; ET-3; PPET3; tmgc48; 114CH19
??[Similar Products]
NCBI Protein Information
endothelin-3
UniProt Protein Name
Endothelin-3
UniProt Synonym Protein Names
Preproendothelin-3; PPET3
Protein Family
Endothelin
UniProt Gene Name
Edn3??[Similar Products]
UniProt Synonym Gene Names
ET-3; PPET3??[Similar Products]
UniProt Entry Name
EDN3_MOUSE
NCBI Summary for EDN3
This gene is a member of the endothelin family whose members encode proteins that act on G protein-coupled receptors. Endothelins are produced as large prepropolypeptide precursors that undergo a first cleavage by a subtilisin serine protease to form an inactive intermediate, which in turn is cleaved again by endothelin-converting enzyme 1 (ECE-1) to yield the active 21 amino acid peptide. This gene encodes a protein which is expressed in neural crest cells (NCC), binds to endothelin receptor b (Ednrb) and plays an essential role in the development of NCC-derived cell lineages including melanocytes and enteric neurons. Mutations in this gene are associated with terminal aganglionosis and white spotted coat in mice and Hirschsprung's disease and Waardenburg syndrome in humans. [provided by RefSeq, Apr 2013]
UniProt Comments for EDN3
EDN3: Endothelins are endothelium-derived vasoconstrictor peptides. Defects in EDN3 are the cause of Hirschsprung disease type 4 (HSCR4); also known as aganglionic megacolon (MGC). A genetic disorder of neural crest development characterized by the absence of intramural ganglion cells in the hindgut; often resulting in intestinal obstruction. Defects in EDN3 are a cause of congenital central hypoventilation syndrome (CCHS); also known as congenital failure of autonomic control or Ondine curse. CCHS is a rare disorder characterized by abnormal control of respiration in the absence of neuromuscular or lung disease, or an identifiable brain stem lesion. A deficiency in autonomic control of respiration results in inadequate or negligible ventilatory and arousal responses to hypercapnia and hypoxemia. Defects in EDN3 are a cause of Waardenburg syndrome type 4 (WS4B); also known as Waardenburg-Shah syndrome. WS4B is characterized by the association of Waardenburg features (depigmentation and deafness) and the absence of enteric ganglia in the distal part of the intestine (Hirschsprung disease). Belongs to the endothelin/sarafotoxin family. 3 isoforms of the human protein are produced by alternative splicing.
Protein type: Secreted; Secreted, signal peptide
Cellular Component: extracellular space; cell; extracellular region; intracellular
Molecular Function: hormone activity
Biological Process: regulation of systemic arterial blood pressure by endothelin; negative regulation of hormone secretion; regulation of neurotransmitter secretion; positive regulation of leukocyte chemotaxis; vein smooth muscle contraction; regulation of cell migration; neuron differentiation; positive regulation of MAP kinase activity; cell surface receptor linked signal transduction; melanocyte differentiation; positive regulation of cell proliferation; regulation of blood vessel size; neural crest cell migration; neutrophil chemotaxis; vasoconstriction; inositol phosphate-mediated signaling; positive regulation of mitosis; positive regulation of hormone secretion; positive regulation of heart rate; peptide hormone secretion; cellular calcium ion homeostasis; regulation of gene expression; regulation of vasoconstriction; regulation of pigmentation during development; positive regulation of cell differentiation
Research Articles on EDN3
1. Enterocolitis causes profound lymphoid depletion in endothelin receptor B- and endothelin 3-null mouse models of Hirschsprung-associated enterocolitis.
Precautions
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Disclaimer
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