Human B9D2 Protein

<strong>Human B9D2 Protein</strong>_x000D_ <strong>Catalog number:</strong> B2011827_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> B9 domain-containing protein 2 protein, ICIS-1 protein, MKS10 protein, MKSR2 protein_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: Parisi M, Glass I. Joubert Syndrome 2003 Jul 9 [updated 2017 Jun 29]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews(®) [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022._x000D_ 2: Okazaki M, Kobayashi T, Chiba S, Takei R, Liang L, Nakayama K, Katoh Y. Formation of the B9-domain protein complex MKS1-B9D2-B9D1 is essential as a diffusion barrier for ciliary membrane proteins Mol Biol Cell. 2020 Sep 15;31(20):2259-2268._x000D_ 3: Dowdle WE, Robinson JF, Kneist A, Sirerol-Piquer MS, Frints SG, Corbit KC, Zaghloul NA, van Lijnschoten G, Mulders L, Verver DE, Zerres K, Reed RR, Attié-Bitach T, Johnson CA, García-Verdugo JM, Katsanis N, Bergmann C, Reiter JF. Disruption of a ciliary B9 protein complex causes Meckel syndrome Am J Hum Genet. 2011 Jul 15;89(1):94-110._x000D_ 4: Guan Y, Liu L, Jia Q, Jin X, Pang Y, Meng F, Zhang X, Shen H. The Role of Cell Growth-Related Gene Copy Number Variation in Autoimmune Thyroid Disease Biol Trace Elem Res. 2020 Jun;195(2):409-416._x000D_ 5: Lange KI, Tsiropoulou S, Kucharska K, Blacque OE. Interpreting the pathogenicity of Joubert syndrome missense variants in Caenorhabditis elegans Dis Model Mech. 2021 Jan 1;14(1):dmm046631._x000D_ 6: Williams CL, Winkelbauer ME, Schafer JC, Michaud EJ, Yoder BK. Functional redundancy of the B9 proteins and nephrocystins in Caenorhabditis elegans ciliogenesis Mol Biol Cell. 2008 May;19(5):2154-68._x000D_ 7: Luo M, He R, Lin Z, Shen Y, Zhang G, Cao Z, Lu C, Meng D, Zhang J, Ma X, Cao M. Novel Compound Heterozygous Variants in MKS1 Leading to Joubert Syndrome Front Genet. 2020 Oct 14;11:576235._x000D_ 8: Zhao C, Malicki J. Nephrocystins and MKS proteins interact with IFT particle and facilitate transport of selected ciliary cargos EMBO J. 2011 May 20;30(13):2532-44._x000D_ 9: Lin T, Ma Y, Zhou D, Sun L, Chen K, Xiang Y, Tong K, Jia C, Jiang K, Liu D, Huang G. Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozygous Mutations of MKS1 Front Genet. 2022 Mar 14;13:843931._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/20301743">10: Gunay-Aygun M, Gahl WA, Heller T. Congenital Hepatic Fibrosis Overview ─ RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY 2008 Dec 9 [updated 2014 Apr 24]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews(®) [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022.</a>_x000D_ _x000D_ <strong>Products Related to Human B9D2 Protein can be found at</strong> <a href="https://moleculardepot.com/product-category/Proteins/"> Proteins</a>