Anti SLC12A3 pAb (ATL-HPA028748 w/enhanced validation)

Catalog No:
ATL-HPA028748-25
$360.00
Application: IHC 
Clonality: Polyclonal 
Host: Rabbit 
Reactivity: Human 
Protein Description: solute carrier family 12 (sodium/chloride transporter), member 3
Gene Name: SLC12A3
Alternative Gene Name: NCCT
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000031766: 90%, ENSRNOG00000057072: 90%
Entrez Gene ID: 6559
Uniprot ID: P55017
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.

Cognate Antibody/Antigen for Anti SLC12A3 pAb (ATL-HPA028748 w/enhanced validation)
Antigen PrEST Antigen SLC12A3 (ATL-APrEST86793)
Documents & Links for Anti SLC12A3 pAb (ATL-HPA028748 w/enhanced validation)
Datasheet Anti SLC12A3 pAb (ATL-HPA028748 w/enhanced validation) Datasheet (External Link)
Vendor Page Anti SLC12A3 pAb (ATL-HPA028748 w/enhanced validation) at Atlas

Documents & Links for Anti SLC12A3 pAb (ATL-HPA028748 w/enhanced validation)
Datasheet Anti SLC12A3 pAb (ATL-HPA028748 w/enhanced validation) Datasheet (External Link)
Vendor Page Anti SLC12A3 pAb (ATL-HPA028748 w/enhanced validation)

Citations for Anti SLC12A3 pAb (ATL-HPA028748 w/enhanced validation) – 11 Found
Conserved and Divergent Molecular and Anatomic Features of Human and Mouse Nephron Patterning.
J Am Soc Nephrol. 2018 Mar;29(3):825-840. doi: 10.1681/ASN.2017091036. Epub 2018 Feb 15.  PubMed
Reduced Abd-B Hox function during kidney development results in lineage infidelity.
Dev Biol. 2018 Jun 15;438(2):84-93. doi: 10.1016/j.ydbio.2018.03.020. Epub 2018 Mar 26.  PubMed
EED, a member of the polycomb group, is required for nephron differentiation and the maintenance of nephron progenitor cells.
Development. 2018 Jul 18;145(14):dev157149. doi: 10.1242/dev.157149.  PubMed
H(+)-ATPase B1 subunit localizes to thick ascending limb and distal convoluted tubule of rodent and human kidney.
Am J Physiol Renal Physiol. 2018 Sep 1;315(3):F429-F444. doi: 10.1152/ajprenal.00539.2017. Epub 2018 Jul 11.  PubMed
Hnf4a Is Required for the Development of Cdh6-Expressing Progenitors into Proximal Tubules in the Mouse Kidney.
J Am Soc Nephrol. 2020 Nov;31(11):2543-2558. doi: 10.1681/ASN.2020020184. Epub 2020 Aug 6.  PubMed
Long-term Clinical Course after Living Kidney Donation by a Patient with Gitelman Syndrome Harboring a Compound Heterozygous Mutation of the SLC12A3 Gene.
Intern Med. 2021 May 15;60(10):1567-1572. doi: 10.2169/internalmedicine.5977-20. Epub 2020 Dec 15.  PubMed
Affinity proteomics reveals elevated muscle proteins in plasma of children with cerebral malaria.
PLoS Pathog. 2014 Apr 17;10(4):e1004038. doi: 10.1371/journal.ppat.1004038. eCollection 2014 Apr.  PubMed
Hnf4a deletion in the mouse kidney phenocopies Fanconi renotubular syndrome.
JCI Insight. 2018 Jul 26;3(14):e97497. doi: 10.1172/jci.insight.97497. eCollection 2018 Jul 26.  PubMed
β-catenin regulates the formation of multiple nephron segments in the mouse kidney.
Sci Rep. 2019 Nov 4;9(1):15915. doi: 10.1038/s41598-019-52255-w.  PubMed
Monkeys mutant for PKD1 recapitulate human autosomal dominant polycystic kidney disease.
Nat Commun. 2019 Dec 11;10(1):5517. doi: 10.1038/s41467-019-13398-6.  PubMed
In Situ Classification of Cell Types in Human Kidney Tissue Using 3D Nuclear Staining.
Cytometry A. 2021 Jul;99(7):707-721. doi: 10.1002/cyto.a.24274. Epub 2020 Dec 13.  PubMed