NB200-316
antibody from Novus Biologicals
Targeting: CELF1
BRUNOL2, CUG-BP, CUGBP, CUGBP1, EDEN-BP, hNab50, NAB50, NAPOR
Antibody data
- Antibody Data
- Antigen structure
- References [11]
- Comments [0]
- Validations
- Western blot [2]
- Immunohistochemistry [1]
- Flow cytometry [1]
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Validation data
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- Product number
- NB200-316 - Provider product page
- Provider
- Novus Biologicals
- Proper citation
- Novus Cat#NB200-316, RRID:AB_2086153
- Product name
- Mouse Monoclonal CUGBP1/CELF1 Antibody
- Antibody type
- Monoclonal
- Description
- Protein G purified.
- Reactivity
- Human, Mouse, Rat, Bovine, Porcine, Rabbit, Simian
- Host
- Mouse
- Isotype
- IgG
- Vial size
- 0.1 ml
- Concentration
- 1 mg/ml
- Storage
- Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
Submitted references Smaug/SAMD4A restores translational activity of CUGBP1 and suppresses CUG-induced myopathy.
Bcl-x pre-mRNA splicing regulates brain injury after neonatal hypoxia-ischemia.
CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1.
Ectopic expression of CGG containing mRNA is neurotoxic in mammals.
Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy.
Inactivation of CUG-BP1/CELF1 causes growth, viability, and spermatogenesis defects in mice.
Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy.
Nuclear RNA foci in the heart in myotonic dystrophy.
Ribonuclear inclusions in skeletal muscle in myotonic dystrophy types 1 and 2.
Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy.
A family of human RNA-binding proteins related to the Drosophila Bruno translational regulator.
de Haro M, Al-Ramahi I, Jones KR, Holth JK, Timchenko LT, Botas J
PLoS genetics 2013 Apr;9(4):e1003445
PLoS genetics 2013 Apr;9(4):e1003445
Bcl-x pre-mRNA splicing regulates brain injury after neonatal hypoxia-ischemia.
Xiao Q, Ford AL, Xu J, Yan P, Lee KY, Gonzales E, West T, Holtzman DM, Lee JM
The Journal of neuroscience : the official journal of the Society for Neuroscience 2012 Sep 26;32(39):13587-96
The Journal of neuroscience : the official journal of the Society for Neuroscience 2012 Sep 26;32(39):13587-96
CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1.
Ward AJ, Rimer M, Killian JM, Dowling JJ, Cooper TA
Human molecular genetics 2010 Sep 15;19(18):3614-22
Human molecular genetics 2010 Sep 15;19(18):3614-22
Ectopic expression of CGG containing mRNA is neurotoxic in mammals.
Hashem V, Galloway JN, Mori M, Willemsen R, Oostra BA, Paylor R, Nelson DL
Human molecular genetics 2009 Jul 1;18(13):2443-51
Human molecular genetics 2009 Jul 1;18(13):2443-51
Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy.
Orengo JP, Chambon P, Metzger D, Mosier DR, Snipes GJ, Cooper TA
Proceedings of the National Academy of Sciences of the United States of America 2008 Feb 19;105(7):2646-51
Proceedings of the National Academy of Sciences of the United States of America 2008 Feb 19;105(7):2646-51
Inactivation of CUG-BP1/CELF1 causes growth, viability, and spermatogenesis defects in mice.
Kress C, Gautier-Courteille C, Osborne HB, Babinet C, Paillard L
Molecular and cellular biology 2007 Feb;27(3):1146-57
Molecular and cellular biology 2007 Feb;27(3):1146-57
Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy.
Lin X, Miller JW, Mankodi A, Kanadia RN, Yuan Y, Moxley RT, Swanson MS, Thornton CA
Human molecular genetics 2006 Jul 1;15(13):2087-97
Human molecular genetics 2006 Jul 1;15(13):2087-97
Nuclear RNA foci in the heart in myotonic dystrophy.
Mankodi A, Lin X, Blaxall BC, Swanson MS, Thornton CA
Circulation research 2005 Nov 25;97(11):1152-5
Circulation research 2005 Nov 25;97(11):1152-5
Ribonuclear inclusions in skeletal muscle in myotonic dystrophy types 1 and 2.
Mankodi A, Teng-Umnuay P, Krym M, Henderson D, Swanson M, Thornton CA
Annals of neurology 2003 Dec;54(6):760-8
Annals of neurology 2003 Dec;54(6):760-8
Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy.
Savkur RS, Philips AV, Cooper TA
Nature genetics 2001 Sep;29(1):40-7
Nature genetics 2001 Sep;29(1):40-7
A family of human RNA-binding proteins related to the Drosophila Bruno translational regulator.
Good PJ, Chen Q, Warner SJ, Herring DC
The Journal of biological chemistry 2000 Sep 15;275(37):28583-92
The Journal of biological chemistry 2000 Sep 15;275(37):28583-92
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Supportive validation
- Submitted by
- Novus Biologicals (provider)
- Main image
- Experimental details
- Simple Western: CUGBP1 Antibody (3B1) [NB200-316] - Simple Western lane view shows a specific band for CUGBP1 in 0.5 mg/ml of HeLa lysate. This experiment was performed under reducing conditions using the 12-230 kDa separation system.
- Submitted by
- Novus Biologicals (provider)
- Main image
- Experimental details
- Western Blot: CUGBP1 Antibody (3B1) [NB200-316] - Detection of CUG-BP1 in several cell lysates.
Supportive validation
- Submitted by
- Novus Biologicals (provider)
- Main image
- Experimental details
- Immunohistochemistry-Paraffin: CUGBP1/CELF1 Antibody (3B1) [NB200-316] - IHC analysis of a formalin fixed paraffin-embedded (FFPE) human spleen using 1:100 conc. of CUGBP1/CELF1 antibody on a Bond Rx autostainer (Leica Biosystems). The assay involved 30 minutes of heat induced antigen retrieval (HIER) using 10mM sodium citrate buffer (pH 9.0) and endogenous peroxidase quenching with peroxide block. The sections were incubated with primary antibody for 15 minutes and Bond Polymer Refine Detection (Leica Biosystems) with DAB was used for signal development followed by counterstaining with hematoxylin. Nuclear staining was observed in lymphocytes.
Supportive validation
- Submitted by
- Novus Biologicals (provider)
- Main image
- Experimental details
- Flow Cytometry: CUGBP1 Antibody (3B1) [NB200-316] - Intracellular flow cytometric staining of 1 x 10^6 MCF-7 cells using CUGBP1 antibody (dark blue). Isotype control shown in orange. An antibody concentration of 1 ug/1x10^6 cells was used.