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Home cDNA Clone TrueORF All WNK4 ORF Clones

WNK4 (NM_032387) Human cDNA ORF Clone

Specifications Citations Clone of Other Species Product Documents
Cat. No. Description Price Availability  
RG223269 GFP-tagged ORF clone of Homo sapiens WNK lysine deficient protein kinase 4 (WNK4) as transfection-ready DNA, 10µg
$860
2-3 weeks

$50 off anti-DDK and other anti-tag antibodies till June 30th, 2013

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Also for WNK4 (NM_032387)
cDNA Clone shRNA/siRNA Lysate Protein Antibody
TrueORF Data for RG223269
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Vector: pCMV6-AC-GFP   Change vector? Tag: C-terminal TurboGFP
Sequence Data: ORF Nucleotide Sequence
Protein Sequence
ORF Size: 3732 bp
Restriction Sites: SgfI-RsrII     Cloning Scheme for this gene     Plasmid Map Plasmid Map
OTI Annotation: This clone was engineered to express the complete ORF with an expression tag.
OTI Disclaimer: The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
Product Components: The ORF clone is ion-exchange column purified, transfection-ready dried plasmid DNA, and shipped with 2 vector sequencing primers.
Protein Families: Protein KinaseDruggable Genome
* The lysates used for this WB picture contain the overexpressed empty vector or the Myc-DDK tagged ORF clone.

Reference Data
RefSeq: NM_032387.3, NP_115763
RefSeq Size: 4147 RefSeq ORF: 3732
Synonyms : PHA2B; PRKWNK4
LocusID: 65266 Cytogenetic: 17q21
Summary: This gene encodes a member of the WNK family of serine-threonine protein kinases. The kinase is part of the tight junction complex in kidney cells, and regulates the balance between NaCl reabsorption and K(+) secretion. The kinase regulates the activities of several types of ion channels, cotransporters, and exchangers involved in electrolyte flux in epithelial cells. Mutations in this gene result in pseudohypoaldosteronism type IIB.[provided by RefSeq, Sep 2009].

 

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