Antibody data
- Antibody Data
- Antigen structure
- References [10]
- Comments [0]
- Validations
- Western blot [1]
- Immunohistochemistry [1]
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Validation data
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- Product number
- ABIN152898 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Scavenger Receptor Class B, Member 2 (SCARB2) (C-Term) antibody
- Antibody type
- Polyclonal
- Description
- Unpurified
- Reactivity
- Human, Mouse, Rat, Canine, Simian
- Host
- Rabbit
- Epitope
- C-Term
- Vial size
- 0.1 mL
- Storage
- Aliquot and store at -20°C or -80°C. Avoid freeze-thaw cycles.
- Handling
- Avoid freeze-thaw cycles
Submitted references Mutation in VPS33A affects metabolism of glycosaminoglycans: a new type of mucopolysaccharidosis with severe systemic symptoms.
Evaluation of AAV-mediated Gene Therapy for Central Nervous System Disease in Canine Mucopolysaccharidosis VII.
Lysosome associated membrane proteins maintain pancreatic acinar cell homeostasis: LAMP-2 deficient mice develop pancreatitis.
Tight junctional localization of claudin-16 is regulated by syntaxin 8 in renal tubular epithelial cells.
Action myoclonus-renal failure syndrome: diagnostic applications of activity-based probes and lipid analysis.
High-density lipoprotein endocytosis in endothelial cells.
Whole body correction of mucopolysaccharidosis IIIA by intracerebrospinal fluid gene therapy.
Abnormal Processing of Autophagosomes in Transformed B Lymphocytes from SCARB2-Deficient Subjects.
Expression of the transmembrane lysosomal protein SCARB2/Limp-2 in renin secretory granules controls renin release.
A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome.
Kondo H, Maksimova N, Otomo T, Kato H, Imai A, Asano Y, Kobayashi K, Nojima S, Nakaya A, Hamada Y, Irahara K, Gurinova E, Sukhomyasova A, Nogovicina A, Savvina M, Yoshimori T, Ozono K, Sakai N
Human molecular genetics 2017 Jan 1;26(1):173-183
Human molecular genetics 2017 Jan 1;26(1):173-183
Evaluation of AAV-mediated Gene Therapy for Central Nervous System Disease in Canine Mucopolysaccharidosis VII.
Gurda BL, De Guilhem De Lataillade A, Bell P, Zhu Y, Yu H, Wang P, Bagel J, Vite CH, Sikora T, Hinderer C, Calcedo R, Yox AD, Steet RA, Ruane T, O'Donnell P, Gao G, Wilson JM, Casal M, Ponder KP, Haskins ME
Molecular therapy : the journal of the American Society of Gene Therapy 2016 Feb;24(2):206-216
Molecular therapy : the journal of the American Society of Gene Therapy 2016 Feb;24(2):206-216
Lysosome associated membrane proteins maintain pancreatic acinar cell homeostasis: LAMP-2 deficient mice develop pancreatitis.
Mareninova OA, Sendler M, Malla SR, Yakubov I, French SW, Tokhtaeva E, Vagin O, Oorschot V, Lüllmann-Rauch R, Blanz J, Dawson D, Klumperman J, Lerch MM, Mayerle J, Gukovsky I, Gukovskaya AS
Cellular and molecular gastroenterology and hepatology 2015 Nov 1;1(6):678-694
Cellular and molecular gastroenterology and hepatology 2015 Nov 1;1(6):678-694
Tight junctional localization of claudin-16 is regulated by syntaxin 8 in renal tubular epithelial cells.
Ikari A, Tonegawa C, Sanada A, Kimura T, Sakai H, Hayashi H, Hasegawa H, Yamaguchi M, Yamazaki Y, Endo S, Matsunaga T, Sugatani J
The Journal of biological chemistry 2014 May 9;289(19):13112-23
The Journal of biological chemistry 2014 May 9;289(19):13112-23
Action myoclonus-renal failure syndrome: diagnostic applications of activity-based probes and lipid analysis.
Gaspar P, Kallemeijn WW, Strijland A, Scheij S, Van Eijk M, Aten J, Overkleeft HS, Balreira A, Zunke F, Schwake M, Sá Miranda C, Aerts JM
Journal of lipid research 2014 Jan;55(1):138-45
Journal of lipid research 2014 Jan;55(1):138-45
High-density lipoprotein endocytosis in endothelial cells.
Fruhwürth S, Pavelka M, Bittman R, Kovacs WJ, Walter KM, Röhrl C, Stangl H
World journal of biological chemistry 2013 Nov 26;4(4):131-40
World journal of biological chemistry 2013 Nov 26;4(4):131-40
Whole body correction of mucopolysaccharidosis IIIA by intracerebrospinal fluid gene therapy.
Haurigot V, Marcó S, Ribera A, Garcia M, Ruzo A, Villacampa P, Ayuso E, Añor S, Andaluz A, Pineda M, García-Fructuoso G, Molas M, Maggioni L, Muñoz S, Motas S, Ruberte J, Mingozzi F, Pumarola M, Bosch F
The Journal of clinical investigation 2013 Jul 1;
The Journal of clinical investigation 2013 Jul 1;
Abnormal Processing of Autophagosomes in Transformed B Lymphocytes from SCARB2-Deficient Subjects.
Gleich K, Desmond MJ, Lee D, Berkovic SF, Dibbens LM, Katerelos M, Bayly MA, Fraser SA, Martinello P, Vears DF, Mount P, Power DA
BioResearch open access 2013 Feb;2(1):40-6
BioResearch open access 2013 Feb;2(1):40-6
Expression of the transmembrane lysosomal protein SCARB2/Limp-2 in renin secretory granules controls renin release.
Lee D, Desmond MJ, Fraser SA, Katerelos M, Gleich K, Berkovic SF, Power DA
Nephron. Experimental nephrology 2012;122(3-4):103-13
Nephron. Experimental nephrology 2012;122(3-4):103-13
A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome.
Balreira A, Gaspar P, Caiola D, Chaves J, Beirão I, Lima JL, Azevedo JE, Miranda MC
Human molecular genetics 2008 Jul 15;17(14):2238-43
Human molecular genetics 2008 Jul 15;17(14):2238-43
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Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- WB
Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- IHC