Human BSND Protein

<strong>Human BSND Protein</strong>_x000D_ <strong>Catalog number:</strong> B2011651_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 20 µg_x000D_ <strong>Molecular Weight or Concentration:</strong> 250 µg/mL_x000D_ <strong>Supplied as:</strong> Solution_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20 °C_x000D_ <strong>Keywords:</strong> Barttin protein, BART protein, DFNB73 protein, BSND_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Viering DHHM, de Baaij JHF, Walsh SB, Kleta R, Bockenhauer D. Genetic causes of hypomagnesemia, a clinical overview Pediatr Nephrol. 2017 Jul;32(7):1123-1135._x000D_ 2: Nomura N, Shoda W, Uchida S. Clinical importance of potassium intake and molecular mechanism of potassium regulation Clin Exp Nephrol. 2019 Oct;23(10):1175-1180._x000D_ 3: Planells-Cases R, Jentsch TJ. Chloride channelopathies Biochim Biophys Acta. 2009 Mar;1792(3):173-89._x000D_ 4: Shinmura K, Kato H, Kawanishi Y, Kamo T, Inoue Y, Yoshimura K, Sugiyama K, Misawa K, Hosokawa S, Mineta H, Sugimura H. BSND is a Novel Immunohistochemical Marker for Oncocytic Salivary Gland Tumors Pathol Oncol Res. 2018 Apr;24(2):439-444._x000D_ 5: Iqbal H, Sarfaraz T, Anjum F, Anwar Z, Mir A. Identification of missense mutation (I12T) in the BSND gene and bioinformatics analysis J Biomed Biotechnol. 2011;2011:304612._x000D_ 6: Ke P, Qian L, Zhou Y, Feng L, Zhang Z, Zheng C, Chen M, Huang X, Wu X. Identification of hub genes and transcription factor-miRNA-mRNA pathways in mice and human renal ischemia-reperfusion injury PeerJ. 2021 Oct 26;9:e12375._x000D_ 7: Sile S, Gillani NB, Velez DR, Vanoye CG, Yu C, Byrne LM, Gainer JV, Brown NJ, Williams SM, George AL Jr. Functional BSND variants in essential hypertension Am J Hypertens. 2007 Nov;20(11):1176-1182._x000D_ 8: Riazuddin S, Anwar S, Fischer M, Ahmed ZM, Khan SY, Janssen AG, Zafar AU, Scholl U, Husnain T, Belyantseva IA, Friedman PL, Riazuddin S, Friedman TB, Fahlke C. Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome Am J Hum Genet. 2009 Aug;85(2):273-80._x000D_ 9: Shinmura K, Igarashi H, Kato H, Koda K, Ogawa H, Takahashi S, Otsuki Y, Yoneda T, Kawanishi Y, Funai K, Takayama T, Ozono S, Sugimura H. BSND and ATP6V1G3: Novel Immunohistochemical Markers for Chromophobe Renal Cell Carcinoma Medicine (Baltimore). 2015 Jun;94(24):e989._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/11687798">10: Birkenhäger R, Otto E, Schürmann MJ, Vollmer M, Ruf EM, Maier-Lutz I, Beekmann F, Fekete A, Omran H, Feldmann D, Milford DV, Jeck N, Konrad M, Landau D, Knoers NV, Antignac C, Sudbrak R, Kispert A, Hildebrandt F. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure Nat Genet. 2001 Nov;29(3):310-4. </a>_x000D_ _x000D_ <strong>Products Related to Human BSND Protein can be found at</strong> <a href="https://moleculardepot.com/product-category/Proteins/"> Proteins</a>