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Details for Product No. ABIN565080

TAR DNA Binding Protein (TARDBP) (AA 1-260) antibody

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Antigen
Synonyms ALS10, TDP-43, Tdp43, C85084, 1190002A23Rik, wu:fb77f02, wu:fc52g10, TARDBP, TDP43, DKFZp459I2127, tardbp
Epitope
»Alternatives AA 1-260
Reactivity
»Alternatives Human
Host
»Alternatives Mouse
Clonality (Clone) Monoclonal ()
Conjugate
»Alternatives Un-conjugated
Application
»Alternatives Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB), ELISA, Immunoprecipitation (IP), RNA Interference (RNAi)
Pubmed 85 references available
Catalog no. ABIN565080
Quantity 100 µg
Price
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Immunogen TARDBP (AAH01487.1, 1 a.a. ~ 260 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Immunogen sequence: MSEYIRVTEDENDEPIEIPS EDDGTVLLSTVTAQFPGACG LRYRNPVSQCMRGVRLVEGI LHAPDAGWGNLVYVVNYPKD NKRKMDETDASSAVKVKRAV QKTSDLIVLGLPWKTTEQDL KEYFSTFGEVLMVQVKKDLK TGHSKGFGFVRFTEYETQVK VMSQRHMIDGRWCDCKLPNS KQSQDEPLRSRKVFVGRCTE DMTEDELREFFSQYGDVMDV FIPKPFRAFAFVTFADDQIA QSLCGEDLIIKGISVHISNA
Clone 2E2-D3
Isotype IgG1 kappa
Characteristics Mouse monoclonal antibody raised against a full length recombinant TARDBP.
Alternative Name TARDBP
Background Gene: TAR DNA binding protein
Synonyms: ALS10, TDP-43
Gene ID 23435, BC001487
Research Area Chromatin and Nuclear Signaling, Transcription Factors, DNA/RNA, Hormones, Cytokines
Application Notes Application specialization: Cell lysate, Recombinant protein, Transfected lysate
Restrictions For Research Use only
Buffer 1x PBS, pH 7.2
Storage -20 °C
Storage Comment Store at -20 °C or lower. Aliquot to avoid repeated freezing and thawing.
Product cited in: Arai, Hasegawa, Akiyama et al.: "TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis." in: Biochemical and biophysical research communications, Vol. 351, Issue 3, pp. 602-11, 2006 (PubMed).

Neumann, Mackenzie, Cairns et al.: "TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations." in: Journal of neuropathology and experimental neurology, Vol. 66, Issue 2, pp. 152-7, 2007 (PubMed).

Tan, Eguchi, Tagawa et al.: "TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation." in: Acta neuropathologica, Vol. 113, Issue 5, pp. 535-42, 2007 (PubMed).

Neumann, Kwong, Truax et al.: "TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusions." in: Journal of neuropathology and experimental neurology, Vol. 66, Issue 3, pp. 177-83, 2007 (PubMed).

Fukuda, Yamagata, Fujiyama et al.: "DEAD-box RNA helicase subunits of the Drosha complex are required for processing of rRNA and a subset of microRNAs." in: Nature cell biology, Vol. 9, Issue 5, pp. 604-11, 2007 (PubMed).

Hasegawa, Arai, Akiyama et al.: "TDP-43 is deposited in the Guam parkinsonism-dementia complex brains." in: Brain : a journal of neurology, Vol. 130, Issue Pt 5, pp. 1386-94, 2007 (PubMed).

Mackenzie, Bigio, Ince et al.: "Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations." in: Annals of neurology, Vol. 61, Issue 5, pp. 427-34, 2007 (PubMed).

Amador-Ortiz, Lin, Ahmed et al.: "TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease." in: Annals of neurology, Vol. 61, Issue 5, pp. 435-45, 2007 (PubMed).

Zhang, Tan, Mori et al.: "TDP-43-immunoreactive neuronal and glial inclusions in the neostriatum in amyotrophic lateral sclerosis with and without dementia." in: Acta neuropathologica, Vol. 115, Issue 1, pp. 115-22, 2007 (PubMed).

Shankaran, Capell, Hruscha et al.: "Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion." in: The Journal of biological chemistry, Vol. 283, Issue 3, pp. 1744-53, 2008 (PubMed).

Kovacs, Pittman, Revesz et al.: "MAPT S305I mutation: implications for argyrophilic grain disease." in: Acta neuropathologica, Vol. 116, Issue 1, pp. 103-18, 2008 (PubMed).

Sanelli, Xiao, Horne et al.: "Evidence that TDP-43 is not the major ubiquitinated target within the pathological inclusions of amyotrophic lateral sclerosis." in: Journal of neuropathology and experimental neurology, Vol. 66, Issue 12, pp. 1147-53, 2007 (PubMed).

Beck, Rohrer, Campbell et al.: "A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series." in: Brain : a journal of neurology, Vol. 131, Issue Pt 3, pp. 706-20, 2008 (PubMed).

Zhang, Tanji, Mori et al.: "Epitope mapping of 2E2-D3, a monoclonal antibody directed against human TDP-43." in: Neuroscience letters, Vol. 434, Issue 2, pp. 170-4, 2008 (PubMed).

Winton, Igaz, Wong et al.: "Disturbance of nuclear and cytoplasmic TAR DNA-binding protein (TDP-43) induces disease-like redistribution, sequestration, and aggregate formation." in: The Journal of biological chemistry, Vol. 283, Issue 19, pp. 13302-9, 2008 (PubMed).

Johnson, McCaffery, Lindquist et al.: "A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 105, Issue 17, pp. 6439-44, 2008 (PubMed).

Foulds, McAuley, Gibbons et al.: "TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer's disease and frontotemporal lobar degeneration." in: Acta neuropathologica, Vol. 116, Issue 2, pp. 141-6, 2008 (PubMed).

Igaz, Kwong, Xu et al.: "Enrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosis." in: The American journal of pathology, Vol. 173, Issue 1, pp. 182-94, 2008 (PubMed).

Sleegers, Kumar-Singh, Cruts et al.: "Molecular pathogenesis of frontotemporal lobar degeneration: basic science seminar in neurology." in: Archives of neurology, Vol. 65, Issue 6, pp. 700-4, 2008 (PubMed).

Mori, Tanji, Zhang et al.: "Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia." in: Acta neuropathologica, Vol. 116, Issue 2, pp. 193-203, 2008 (PubMed).

Lin, Dickson: "Ultrastructural localization of TDP-43 in filamentous neuronal inclusions in various neurodegenerative diseases." in: Acta neuropathologica, Vol. 116, Issue 2, pp. 205-13, 2008 (PubMed).

Weihl, Temiz, Miller et al.: "TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia." in: Journal of neurology, neurosurgery, and psychiatry, Vol. 79, Issue 10, pp. 1186-9, 2008 (PubMed).

Kovacs, Majtenyi, Spina et al.: "White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration." in: Journal of neuropathology and experimental neurology, Vol. 67, Issue 10, pp. 963-75, 2008 (PubMed).

Miklossy, Steele, Yu et al.: "Enduring involvement of tau, beta-amyloid, alpha-synuclein, ubiquitin and TDP-43 pathology in the amyotrophic lateral sclerosis/parkinsonism-dementia complex of Guam (ALS/PDC)." in: Acta neuropathologica, Vol. 116, Issue 6, pp. 625-37, 2008 (PubMed).

Skoglund, Brundin, Olofsson et al.: "Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation." in: Neurogenetics, Vol. 10, Issue 1, pp. 27-34, 2009 (PubMed).

Nishihira, Tan, Hoshi et al.: "Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology." in: Acta neuropathologica, Vol. 117, Issue 1, pp. 45-53, 2008 (PubMed).

Kasai, Tokuda, Ishigami et al.: "Increased TDP-43 protein in cerebrospinal fluid of patients with amyotrophic lateral sclerosis." in: Acta neuropathologica, Vol. 117, Issue 1, pp. 55-62, 2008 (PubMed).

Seppänen, Pikkarainen, Hartikainen et al.: "Expression of collagen XVII and ubiquitin-binding protein p62 in motor neuron disease." in: Brain research, Vol. 1247, pp. 171-7, 2008 (PubMed).

Steinacker, Hendrich, Sperfeld et al.: "TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis." in: Archives of neurology, Vol. 65, Issue 11, pp. 1481-7, 2008 (PubMed).

Schwab, Arai, Hasegawa et al.: "Colocalization of transactivation-responsive DNA-binding protein 43 and huntingtin in inclusions of Huntington disease." in: Journal of neuropathology and experimental neurology, Vol. 67, Issue 12, pp. 1159-65, 2008 (PubMed).

Moisse, Volkening, Leystra-Lantz et al.: "Divergent patterns of cytosolic TDP-43 and neuronal progranulin expression following axotomy: implications for TDP-43 in the physiological response to neuronal injury." in: Brain research, Vol. 1249, pp. 202-11, 2009 (PubMed).

Clarimón, Molina-Porcel, Gómez-Isla et al.: "Early-onset familial lewy body dementia with extensive tauopathy: a clinical, genetic, and neuropathological study." in: Journal of neuropathology and experimental neurology, Vol. 68, Issue 1, pp. 73-82, 2009 (PubMed).

Igaz, Kwong, Chen-Plotkin et al.: "Expression of TDP-43 C-terminal Fragments in Vitro Recapitulates Pathological Features of TDP-43 Proteinopathies." in: The Journal of biological chemistry, Vol. 284, Issue 13, pp. 8516-24, 2009 (PubMed).

Rollinson, Rizzu, Sikkink et al.: "Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration." in: Neurobiology of aging, Vol. 30, Issue 4, pp. 656-65, 2009 (PubMed).

Olivé, Janué, Moreno et al.: "TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies." in: Journal of neuropathology and experimental neurology, Vol. 68, Issue 3, pp. 262-73, 2009 (PubMed).

Gitcho, Strider, Carter et al.: "VCP mutations causing frontotemporal lobar degeneration disrupt localization of TDP-43 and induce cell death." in: The Journal of biological chemistry, Vol. 284, Issue 18, pp. 12384-98, 2009 (PubMed).

Humayun, Gohar, Volkening et al.: "The complement factor C5a receptor is upregulated in NFL-/- mouse motor neurons." in: Journal of neuroimmunology, Vol. 210, Issue 1-2, pp. 52-62, 2009 (PubMed).

Velakoulis, Walterfang, Mocellin et al.: "Frontotemporal dementia presenting as schizophrenia-like psychosis in young people: clinicopathological series and review of cases." in: The British journal of psychiatry : the journal of mental science, Vol. 194, Issue 4, pp. 298-305, 2009 (PubMed).

Moisse, Mepham, Volkening et al.: "Cytosolic TDP-43 expression following axotomy is associated with caspase 3 activation in NFL-/- mice: support for a role for TDP-43 in the physiological response to neuronal injury." in: Brain research, Vol. 1296, pp. 176-86, 2009 (PubMed).

Velakoulis, Walterfang, Mocellin et al.: "Abnormal hippocampal distribution of TDP-43 in patients with-late onset psychosis." in: The Australian and New Zealand journal of psychiatry, Vol. 43, Issue 8, pp. 739-45, 2009 (PubMed).

Foulds, Davidson, Mishra et al.: "Plasma phosphorylated-TDP-43 protein levels correlate with brain pathology in frontotemporal lobar degeneration." in: Acta neuropathologica, Vol. 118, Issue 5, pp. 647-58, 2010 (PubMed).

Nishimoto, Ito, Yagi et al.: "Characterization of alternative isoforms and inclusion body of the TAR DNA-binding protein-43." in: The Journal of biological chemistry, Vol. 285, Issue 1, pp. 608-19, 2009 (PubMed).

Fiesel, Voigt, Weber et al.: "Knockdown of transactive response DNA-binding protein (TDP-43) downregulates histone deacetylase 6." in: The EMBO journal, Vol. 29, Issue 1, pp. 209-21, 2010 (PubMed).

Zhang, Tanji, Yoshida et al.: "Alteration of biochemical and pathological properties of TDP-43 protein by a lipid mediator, 15-deoxy-Delta(12,14)-prostaglandin J(2)." in: Experimental neurology, Vol. 222, Issue 2, pp. 296-303, 2010 (PubMed).

Wils, Kleinberger, Janssens et al.: "TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Issue 8, pp. 3858-63, 2010 (PubMed).

Ilieva, Naudí, Kichev et al.: "Depletion of oxidative and endoplasmic reticulum stress regulators in Pick disease." in: Free radical biology & medicine, Vol. 48, Issue 10, pp. 1302-10, 2010 (PubMed).

Braak, Ludolph, Thal et al.: "Amyotrophic lateral sclerosis: dash-like accumulation of phosphorylated TDP-43 in somatodendritic and axonal compartments of somatomotor neurons of the lower brainstem and spinal cord." in: Acta neuropathologica, Vol. 120, Issue 1, pp. 67-74, 2010 (PubMed).

Ash, Zhang, Roberts et al.: "Neurotoxic effects of TDP-43 overexpression in C. elegans." in: Human molecular genetics, Vol. 19, Issue 16, pp. 3206-18, 2010 (PubMed).

Jansen, Head, van Gool et al.: "The first case of protease-sensitive prionopathy (PSPr) in The Netherlands: a patient with an unusual GSS-like clinical phenotype." in: Journal of neurology, neurosurgery, and psychiatry, Vol. 81, Issue 9, pp. 1052-5, 2010 (PubMed).

Ling, Albuquerque, Han et al.: "ALS-associated mutations in TDP-43 increase its stability and promote TDP-43 complexes with FUS/TLS." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Issue 30, pp. 13318-23, 2010 (PubMed).

Xu, Gendron, Zhang et al.: "Wild-type human TDP-43 expression causes TDP-43 phosphorylation, mitochondrial aggregation, motor deficits, and early mortality in transgenic mice." in: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 30, Issue 32, pp. 10851-9, 2010 (PubMed).

Höftberger, Fink, Aboul-Enein et al.: "Tubulin polymerization promoting protein (TPPP/p25) as a marker for oligodendroglial changes in multiple sclerosis." in: Glia, Vol. 58, Issue 15, pp. 1847-57, 2010 (PubMed).

Wang, Dayton, Henning et al.: "Expansive gene transfer in the rat CNS rapidly produces amyotrophic lateral sclerosis relevant sequelae when TDP-43 is overexpressed." in: Molecular therapy : the journal of the American Society of Gene Therapy, Vol. 18, Issue 12, pp. 2064-74, 2010 (PubMed).

Higashi, Tsuchiya, Araki et al.: "TDP-43 physically interacts with amyotrophic lateral sclerosis-linked mutant CuZn superoxide dismutase." in: Neurochemistry international, Vol. 57, Issue 8, pp. 906-13, 2010 (PubMed).

De Marco, Lupino, Calvo et al.: "Cytoplasmic accumulation of TDP-43 in circulating lymphomonocytes of ALS patients with and without TARDBP mutations." in: Acta neuropathologica, Vol. 121, Issue 5, pp. 611-22, 2011 (PubMed).

Rauramaa, Pikkarainen, Englund et al.: "TAR-DNA binding protein-43 and alterations in the hippocampus." in: Journal of neural transmission (Vienna, Austria : 1996), Vol. 118, Issue 5, pp. 683-9, 2011 (PubMed).

Lashley, Holton, Revesz: "TDP-43 pathology may occur in the BRI2 gene-related dementias." in: Acta neuropathologica, Vol. 121, Issue 4, pp. 559-60, 2011 (PubMed).

Herman, Khandelwal, Stanczyk et al.: "β-amyloid triggers ALS-associated TDP-43 pathology in AD models." in: Brain research, Vol. 1386, pp. 191-9, 2011 (PubMed).

Tian, Huang, Tong et al.: "TDP-43 potentiates alpha-synuclein toxicity to dopaminergic neurons in transgenic mice." in: International journal of biological sciences, Vol. 7, Issue 2, pp. 234-43, 2011 (PubMed).

Che, Jiang, Xie et al.: "Aggregation of the 35-kDa fragment of TDP-43 causes formation of cytoplasmic inclusions and alteration of RNA processing." in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology, Vol. 25, Issue 7, pp. 2344-53, 2011 (PubMed).

Hartikainen, Pikkarainen, Hänninen et al.: "Unusual clinical presentation and neuropathology in two subjects with fused-in sarcoma (FUS) positive inclusions." in: Neuropathology : official journal of the Japanese Society of Neuropathology, Vol. 32, Issue 1, pp. 60-8, 2012 (PubMed).

Pikkarainen, Hartikainen, Soininen et al.: "Distribution and pattern of pathology in subjects with familial or sporadic late-onset cerebellar ataxia as assessed by p62/sequestosome immunohistochemistry." in: Cerebellum (London, England), Vol. 10, Issue 4, pp. 720-31, 2011 (PubMed).

Mundiñano, Caballero, Ordóñez et al.: "Increased dopaminergic cells and protein aggregates in the olfactory bulb of patients with neurodegenerative disorders." in: Acta neuropathologica, Vol. 122, Issue 1, pp. 61-74, 2011 (PubMed).

Rusina, Kovacs, Fiala et al.: "FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases." in: BMC neurology, Vol. 11, pp. 50, 2011 (PubMed).

López-Hernández, Sirisi, Capdevila-Nortes et al.: "Molecular mechanisms of MLC1 and GLIALCAM mutations in megalencephalic leukoencephalopathy with subcortical cysts." in: Human molecular genetics, Vol. 20, Issue 16, pp. 3266-77, 2011 (PubMed).

Azizi, Li, Ströbel et al.: "Identification of c-myc-dependent proteins in the medulloblastoma cell line D425Med." in: Amino acids, Vol. 42, Issue 6, pp. 2149-63, 2012 (PubMed).

Martinez-Saez, Gelpi, Rey et al.: "Hirano body-rich subtypes of Creutzfeldt-Jakob disease." in: Neuropathology and applied neurobiology, Vol. 38, Issue 2, pp. 153-61, 2012 (PubMed).

Swarup, Phaneuf, Bareil et al.: "Pathological hallmarks of amyotrophic lateral sclerosis/frontotemporal lobar degeneration in transgenic mice produced with TDP-43 genomic fragments." in: Brain : a journal of neurology, Vol. 134, Issue Pt 9, pp. 2610-26, 2011 (PubMed).

Wang, Brent, Tomlinson et al.: "The ALS-associated proteins FUS and TDP-43 function together to affect Drosophila locomotion and life span." in: The Journal of clinical investigation, Vol. 121, Issue 10, pp. 4118-26, 2011 (PubMed).

Thom, Liu, Thompson et al.: "Neurofibrillary tangle pathology and Braak staging in chronic epilepsy in relation to traumatic brain injury and hippocampal sclerosis: a post-mortem study." in: Brain : a journal of neurology, Vol. 134, Issue Pt 10, pp. 2969-81, 2011 (PubMed).

Antonell, Gelpi, Sánchez-Valle et al.: "Breakpoint sequence analysis of an AβPP locus duplication associated with autosomal dominant Alzheimer's disease and severe cerebral amyloid angiopathy." in: Journal of Alzheimer's disease : JAD, Vol. 28, Issue 2, pp. 303-8, 2012 (PubMed).

Fiesel, Weber, Supper et al.: "TDP-43 regulates global translational yield by splicing of exon junction complex component SKAR." in: Nucleic acids research, Vol. 40, Issue 6, pp. 2668-82, 2012 (PubMed).

Tsuji, Nonaka, Yamashita et al.: "Epitope mapping of antibodies against TDP-43 and detection of protease-resistant fragments of pathological TDP-43 in amyotrophic lateral sclerosis and frontotemporal lobar degeneration." in: Biochemical and biophysical research communications, Vol. 417, Issue 1, pp. 116-21, 2012 (PubMed).

Huang, Tong, Bi et al.: "Mutant TDP-43 in motor neurons promotes the onset and progression of ALS in rats." in: The Journal of clinical investigation, Vol. 122, Issue 1, pp. 107-18, 2012 (PubMed).

Dayton, Wang, Cain et al.: "Frontotemporal lobar degeneration-related proteins induce only subtle memory-related deficits when bilaterally overexpressed in the dorsal hippocampus." in: Experimental neurology, Vol. 233, Issue 2, pp. 807-14, 2012 (PubMed).

Troakes, Maekawa, Wijesekera et al.: "An MND/ALS phenotype associated with C9orf72 repeat expansion: abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline." in: Neuropathology : official journal of the Japanese Society of Neuropathology, Vol. 32, Issue 5, pp. 505-14, 2012 (PubMed).

Herman, Khandelwal, Rebeck et al.: "Wild type TDP-43 induces neuro-inflammation and alters APP metabolism in lentiviral gene transfer models." in: Experimental neurology, Vol. 235, Issue 1, pp. 297-305, 2012 (PubMed).

Echávarri, Burgmans, Caballero et al.: "Co-occurrence of different pathologies in dementia: implications for dementia diagnosis." in: Journal of Alzheimer's disease : JAD, Vol. 30, Issue 4, pp. 909-17, 2012 (PubMed).

Vilas, Marti, Botta-Orfila et al.: "Pick's pathology in Parkinson's disease with dementia." in: Neuropathology and applied neurobiology, Vol. 38, Issue 7, pp. 737-43, 2012 (PubMed).

Colom-Cadena, Gelpi, Martí et al.: "MAPT H1 haplotype is associated with enhanced α-synuclein deposition in dementia with Lewy bodies." in: Neurobiology of aging, Vol. 34, Issue 3, pp. 936-42, 2012 (PubMed).

Gelpi, Soler Insa, Parchi et al.: "Atypical neuropathological sCJD-MM phenotype with abundant white matter Kuru-type plaques sparing the cerebellar cortex." in: Neuropathology : official journal of the Japanese Society of Neuropathology, 2012 (PubMed).

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López-González, Carmona, Blanco et al.: "Characterization of thorn-shaped astrocytes in white matter of temporal lobe in Alzheimer's disease brains." in: Brain pathology (Zurich, Switzerland), Vol. 23, Issue 2, pp. 144-53, 2013 (PubMed).

Tong, Huang, Bi et al.: "XBP1 depletion precedes ubiquitin aggregation and Golgi fragmentation in TDP-43 transgenic rats." in: Journal of neurochemistry, Vol. 123, Issue 3, pp. 406-16, 2012 (PubMed).

Swarup, Audet, Phaneuf et al.: "Abnormal regenerative responses and impaired axonal outgrowth after nerve crush in TDP-43 transgenic mouse models of amyotrophic lateral sclerosis." in: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 32, Issue 50, pp. 18186-95, 2012 (PubMed).

Alternatives for antigen "TAR DNA Binding Protein (TARDBP)", type "Antibodies"
Hosts (89), (23), (6), (1)
Reactivities (115), (68), (48), (34), (19), (19), (17), (17), (5), (3), (1)
Applications (104), (49), (21), (20), (20), (19), (10), (3), (2), (1)
Conjugates (4), (4), (2), (1), (1), (1), (1), (1), (1), (1), (1), (1), (1), (1)
Epitopes (18), (13), (8), (7), (7), (6), (3), (3), (2), (1), (1), (1)
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