S100 beta (S100B) Mouse Monoclonal Capture Antibody [Clone ID: OTI6A6]

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SKU
TA600560
S100B Capture Mouse Monoclonal antibody, clone OTI6A6
  $458.00
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Specifications
Specifications
Product Data
Clone Name OTI6A6
Application ELISA, LMNX
Reactivity Human
Antibody Host Mouse
Isotype IgG1
Clonality Monoclonal
Immunogen Full length human recombinant protein of human S100B (NP_006263) produced in HEK293T cell.
Buffer PBS (pH 7.3) containing 0.05% sodium azide
Concentration 0.5 mg/ml
Purification Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
Conjugation Unconjugated
Storage Store at -20°C.
Avoid repeat freeze/thaw cycles.
Shipping Blue Ice
Predicted Protein Size 10.7 kDa
Gene Name S100 calcium binding protein B
Database Link
Background The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21; however, this gene is located at 21q22.3. This protein may function in Neurite extension, proliferation of melanoma cells, stimulation of Ca2+ fluxes, inhibition of PKC-mediated phosphorylation, astrocytosis and axonal proliferation, and inhibition of microtubule assembly. Chromosomal rearrangements and altered expression of this gene have been implicated in several neurological, neoplastic, and other types of diseases, including Alzheimer's disease, Down's syndrome, epilepsy, amyotrophic lateral sclerosis, melanoma, and type I diabetes. provided by RefSeq, Jul 2008
Synonyms NEF; S100; S100-B; S100beta
Matched ELISA Pair TA700560
Reference Data
Protein Categories Intracellular Proteins
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Documents
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file-alt Citations

Catch-and-display immunoassay for digital biomarker detection
Liu, Walker, Klaczko et al
Nanoscale Horiz (2026)
AI Summary: OriGene contributed key reagents to this study by providing anti-S100B antibodies (TA700560 and TA600560), anti-GFAP antibody pairs (TA700041 and TA600039), and S100B protein (TP300277), which were essential for developing and validating the Catch-and-Display Immunoassay (CAD-IA) described in the paper.
Snippet: The following reagents and materials were used in this study: anti-S100B (TA700560 and TA600560), anti-GFAP antibody pairs (TA700041 and TA600039), and S100B (TP300277) were all purchased from Origene
Catch-and-Display Immunoassay as an Accessible Platform for Digital Biomarker Detection
Liu, Walker, Klaczko et al
bioRxiv (2026)
AI Summary: OriGene contributed to this study by providing antibody pairs (TA700041 and TA600039) and the S100B protein (TP300277), which were essential reagents for developing and validating the Catch-and-Display Immunoassay platform.
Snippet: body pairs (TA700041 and TA600039), and S100B (TP300277) were all purchased from Origene. GFAP was purchased from Cayman Chemical Company (27353). Non-PEGylated Dragon Green Fluorescent Polystyrene Nanoparticles (200 nm, Streptavidin-Coated, Ext480/Emi520) were obtained from Bangslaboratory (FSDG002). PEGylated DiagNano
Fibroblast-derived tenascin-C promotes Schwann cell migration through β1-integrin dependent pathway during peripheral nerve regeneration
Zhang, Yu, Gu et al
Glia (2016) 64 (3), 374-85 DOI: 10.1002/glia.22934
Cited by 77
AI Summary: In this study, OriGene products, including Tenascin-C (TNC) recombinant protein and TNC siRNA, were used to manipulate TNC expression and investigate its role in promoting Schwann cell migration during peripheral nerve regeneration.
Adenosine A₁ and A₂A receptor-mediated modulation of acetylcholine release in the mice neuromuscular junction
Garcia, Priego, Obis et al
Eur J Neurosci (2013) 38 (2), 2229-41 DOI: 10.1111/ejn.12220
Cited by 35
AI Summary: In this study, OriGene's anti-Adenosine A1 Receptor antibody (Cat# TA322897) and anti-Adenosine A2A Receptor antibody (Cat# TA324112) were used for immunocytochemistry to confirm the presence of A1 and A2A receptors at mouse neuromuscular junctions, enabling the investigation of their roles in modulating acetylcholine release.
Showing 1-4 of 4 papers.
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