Recombinant fragment corresponding to Human ATP10D aa 7-551.Sequence: QQLGFDPPHQSDTRTIYVANRFPQNGLYTPQKFIDNRIISSKYTVWNFVP KNLFEQFRRVANFYFLIIFLVQLMIDTPTSPVTSGLPLFFVITVTAIKQG YEDWLRHNSDNEVNGAPVYVVRSGGLVKTRSKNIRVGDIVRIAKDEIFPA DLVLLSSDRLDGSCHVTTASLDGETNLKTHVA
Conjugate
Unconjugated
Target
Alternative Names
ATP11B; ATPase, class VI, type 11B; ATPase, Class VI, type 11B; probable phospholipid-transporting ATPase IF; ATPIF; ATPIR; KIAA0956; ATPase IR; MGC46576; DKFZp434J238; DKFZp434N1615;
ATP11B (ATPase, class VI, type 11B) is a protein-coding gene. Diseases associated with ATP11B include hypoparathyroidism, and among its related super-pathways are Ion channel transport and SLC-mediated transmembrane transport. GO annotations related to this gene include phospholipid-translocating ATPase activity and magnesium ion binding. An important paralog of this gene is ATP11A.
Pathway
Ion channel transport; Ion transport by P-type ATPases; Transmembrane transport of small molecules;
Custom Antibody Labeling
We offer labeled antibodies using our catalogue antibody products and a broad range of intensely fluorescent dyes and labels including HRP, biotin, ALP, Alexa Fluor® dyes, DyLight® Fluor dyes, R-phycoerythrin (R-PE), at scales from less than 100 μg up to 1 g of IgG antibody. Learn More
Citations
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Nesbit, MA; Bowl, MR; et al. X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase. GENOMICS 84:1060-1070(2004).
Ewetson, A; Wright-Pastusek, AE; et al. Conservation of inter-protein binding sites in RUSH and RFBP, an ATP11B isoform. MOLECULAR AND CELLULAR ENDOCRINOLOGY 292:79-86(2008).
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COA
Certificate of Analysis
