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Western blotAntibody data
- Antibody Data
- Antigen structure
- References [7]
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- Product number
- ABIN965586 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Aquaporin 2 (Collecting Duct) (AQP2) (N-Term) antibody
- Antibody type
- Polyclonal
- Antigen
- Polyclonal antibody produced in rabbits immunizing with a synthetic peptide corresponding to N-terminal residues of human AQP2(aquaporin 2)
- Description
- Purified by antigen-specific affinity chromatography.
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- N-Term
- Vial size
- 0.1 mg
- Storage
- -20°C
Submitted references Relationship between adrenomedullin and vasopressin-aquaporin system under general anesthesia.
The proteasome is involved in the degradation of different aquaporin-2 mutants causing nephrogenic diabetes insipidus.
Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidus.
The role of putative phosphorylation sites in the targeting and shuttling of the aquaporin-2 water channel.
Urinary excretion of aquaporin-2 water channel in diabetic ketoacidosis.
Two novel aquaporin-2 mutations responsible for congenital nephrogenic diabetes insipidus in Chinese families.
Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus.
Ogura T, Morita K, Takeuchi M, Otsuka F, Iwasaki T, Oe K, Matsuura K, Tobe K, Mimura Y, Kishida M, Makino H, Hirakawa M
Hormone research 2003;59(1):30-4
Hormone research 2003;59(1):30-4
The proteasome is involved in the degradation of different aquaporin-2 mutants causing nephrogenic diabetes insipidus.
Hirano K, Zuber C, Roth J, Ziak M
The American journal of pathology 2003 Jul;163(1):111-20
The American journal of pathology 2003 Jul;163(1):111-20
Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidus.
Marr N, Bichet DG, Hoefs S, Savelkoul PJ, Konings IB, De Mattia F, Graat MP, Arthus MF, Lonergan M, Fujiwara TM, Knoers NV, Landau D, Balfe WJ, Oksche A, Rosenthal W, Müller D, Van Os CH, Deen PM
Journal of the American Society of Nephrology : JASN 2002 Sep;13(9):2267-77
Journal of the American Society of Nephrology : JASN 2002 Sep;13(9):2267-77
The role of putative phosphorylation sites in the targeting and shuttling of the aquaporin-2 water channel.
van Balkom BW, Savelkoul PJ, Markovich D, Hofman E, Nielsen S, van der Sluijs P, Deen PM
The Journal of biological chemistry 2002 Nov 1;277(44):41473-9
The Journal of biological chemistry 2002 Nov 1;277(44):41473-9
Urinary excretion of aquaporin-2 water channel in diabetic ketoacidosis.
Kusaka I, Saito T, Nakamura T, Nagasaka S, Ishibashi S, Ishikawa SE
Nephron 2002 May;91(1):167-9
Nephron 2002 May;91(1):167-9
Two novel aquaporin-2 mutations responsible for congenital nephrogenic diabetes insipidus in Chinese families.
Lin SH, Bichet DG, Sasaki S, Kuwahara M, Arthus MF, Lonergan M, Lin YF
The Journal of clinical endocrinology and metabolism 2002 Jun;87(6):2694-700
The Journal of clinical endocrinology and metabolism 2002 Jun;87(6):2694-700
Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus.
Marr N, Bichet DG, Lonergan M, Arthus MF, Jeck N, Seyberth HW, Rosenthal W, van Os CH, Oksche A, Deen PM
Human molecular genetics 2002 Apr 1;11(7):779-89
Human molecular genetics 2002 Apr 1;11(7):779-89
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