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SLC39A13 encodes a member of the LIV-1 subfamily of the ZIP transporter family. Additionally we are shipping Solute Carrier Family 39 (Zinc Transporter), Member 13 Proteins (3) and Solute Carrier Family 39 (Zinc Transporter), Member 13 Kits (1) and many more products for this protein.
Showing 10 out of 26 products:
Human Polyclonal SLC39A13 Primary Antibody for EIA, WB - ABIN783815
Dufner-Beattie, Langmade, Wang, Eide, Andrews: Structure, function, and regulation of a subfamily of mouse zinc transporter genes. in The Journal of biological chemistry 2003
Human Polyclonal SLC39A13 Primary Antibody for ICC, IF - ABIN4354361
Jeong, Walker, Wang, Park, Palmer, Giunta, Rohrbach, Steinmann, Eide: Promotion of vesicular zinc efflux by ZIP13 and its implications for spondylocheiro dysplastic Ehlers-Danlos syndrome. in Proceedings of the National Academy of Sciences of the United States of America 2012
This study concluded that skin fragility due to defective ZIP13 protein may be attributable to impaired extracellular matrix synthesis accompanied by abnormal peripheral TGF-beta (show TGFB1 Antibodies) homeostasis.
The Slc39a13-KO mouse represents a novel animal model linking zinc metabolism, BMP/TGF-beta (show TGFb Antibodies) signaling and connective tissue dysfunction.
The spondylocheiro dysplastic form of Ehlers-Danlos syndrome, in which ZIP13 is defective, is likely due to a failure of iron delivery to the secretory compartments.
Authors demonstrated that both the ZIP13(G64D) and ZIP13(DeltaFLA) protein levels are decreased by degradation via the valosin-containing protein (VCP (show vcp Antibodies))-linked ubiquitin proteasome pathway.
human ZIP13 releases zinc from vesicular stores
Biochemical characterization of human ZIP13 protein: a homo-dimerized zinc transporter involved in the spondylocheiro dysplastic Ehlers-Danlos syndrome.
mutations in the SLC39A13 gene do not account for the Ehlers-Danlos syndrome type VIB (show SEMA6B Antibodies) phenotype
clinical features of 6 patients from 2 consanguineous families with Ehlers-Danlos syndrome-like features caused by a mutation in the zinc transporter gene SLC39A13
This gene encodes a member of the LIV-1 subfamily of the ZIP transporter family. The encoded transmembrane protein functions as a zinc transporter. Mutations in this gene have been associated with the spondylocheiro dysplastic form of Ehlers-Danlos syndrome.
, solute carrier family 39 member 13
, zinc transporter ZIP13
, zrt- and Irt-like protein 13
, LIV-1 subfamily of ZIP zinc transporter 9
, solute carrier family 39 (metal ion transporter), member 13