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- Product number
- ABIN951545 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Claudin 16 (CLDN16) (AA 13-41), (N-Term) antibody
- Antibody type
- Polyclonal
- Description
- Affinity chromatography on Protein A
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- AA 13-41, N-Term
- Vial size
- 0.4 mL
- Storage
- Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Transcriptional regulation of the claudin-16 gene by Mg2+ availability.
Significant elevation of CLDN16 and HAPLN3 gene expression in human breast cancer.
Genetic determinants of extracellular magnesium concentration: analysis of multiple candidate genes, and evidence for association with the estrogen receptor alpha (ESR1) locus.
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family.
Efrati E, Hirsch A, Kladnitsky O, Rozenfeld J, Kaplan M, Zinder O, Zelikovic I
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2010;25(6):705-14
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2010;25(6):705-14
Significant elevation of CLDN16 and HAPLN3 gene expression in human breast cancer.
Kuo SJ, Chien SY, Lin C, Chan SE, Tsai HT, Chen DR
Oncology reports 2010 Sep;24(3):759-66
Oncology reports 2010 Sep;24(3):759-66
Genetic determinants of extracellular magnesium concentration: analysis of multiple candidate genes, and evidence for association with the estrogen receptor alpha (ESR1) locus.
Shuen AY, Wong BY, Wei C, Liu Z, Li M, Cole DE
Clinica chimica acta; international journal of clinical chemistry 2009 Nov;409(1-2):28-32
Clinica chimica acta; international journal of clinical chemistry 2009 Nov;409(1-2):28-32
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family.
Al-Haggar M, Bakr A, Tajima T, Fujieda K, Hammad A, Soliman O, Darwish A, Al-Said A, Yahia S, Abdel-Hady D
Clinical and experimental nephrology 2009 Aug;13(4):288-294
Clinical and experimental nephrology 2009 Aug;13(4):288-294
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