Traumatic Brain Injury Biomarker Antibody Sampler Kit #55016
Product Information
Kit Usage Information
Protocols
- 2837: Western Blotting, Immunohistochemistry (Paraffin), Immunofluorescence
- 3450: Western Blotting, Immunofluorescence, Immunofluorescence
- 7074: Western Blotting
- 13179: Western Blotting, Immunohistochemistry (Paraffin), Immunofluorescence, Immunofluorescence, Flow
- 46687: Western Blotting, Immunohistochemistry (Paraffin), Immunofluorescence, Immunofluorescence
- 65162: Western Blotting, Immunofluorescence, Immunofluorescence, Flow Triton Permeabilization (Rabbit)
- 78896: Western Blotting, Immunohistochemistry (Paraffin), Immunofluorescence, Immunofluorescence
- 80788: Western Blotting, Immunohistochemistry (Leica® Bond™), Immunohistochemistry (Paraffin), Immunofluorescence, Immunofluorescence
- 90393: Western Blotting, Immunohistochemistry (Paraffin), Immunofluorescence, Immunofluorescence
Product Description
The Traumatic Brain Injury Biomarker Antibody Sampler Kit provides an economical means of detecting proteins involved in traumatic brain injury. The kit includes enough antibodies to perform two western blot experiments with each primary antibody.
Specificity / Sensitivity
Each antibody in the Traumatic Brain Injury Biomarker Antibody Sampler Kit detects endogenous levels of its target protein. S100B (E7C3A) Rabbit mAb recognizes human S100B protein and is also reactive with mouse S100B; however, this antibody is not suggested for immunohistochemical analysis of mouse tissues. UCHL1 (D3T2E) XP® Rabbit mAb does not cross-react with other UCH family members. Enolase-2 (E7D7I) Rabbit mAb does not cross-react with human Enolase-1 protein.
Source / Purification
Monoclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding His86 of human S100B protein, Glu450 of human Neurofilament-L protein, Asp430 of human tau protein, Ala185 of human myelin basic protein, Gln53 of human PSD95 protein, residues near the carboxy terminus of human Enolase-2 protein and human UCHL1 protein, and recombinant protein specific to human GFAP protein.
Background
Traumatic brain injury (TBI) is a worldwide health issue that significantly affects the patient as well as their family. Annual total cost of nonfatal TBI in 2016 was $40.6 billion in the United States (1). In addition to acute brain injury, even mild cases, can lead to cognitive impairment and long-term psychiatric changes. More long term, TBI patients exhibit lower resilience to neurodegenerative disease-associated pathology (2). Treatment of TBI is made more difficult due to lack of reliable biomarkers to detect TBI (3). Several proteins are of interest, which are candidates for measurement in blood after TBI. Glial fibrillary acidic protein (GFAP) is an astrocytic intermediate filament protein. As a cytoskeletal protein, GFAP helps provide structural support to astrocytes, which provide metabolic support to neurons and maintains the blood brain barrier. The number and size of astrocytes, in a process called astrogliosis, is also positively correlated with brain injury (4). Also abundantly expressed in astrocytes, S100B is commonly used as an astrocytic marker and is positively correlated with TBI (5). Neurofilament-L (NfL) and tau are part of the neuronal cytoskeleton that provide structure to axons. Axons are covered by a multi-layered membrane called the myelin sheath. Myelin basic protein (MBP) is enriched in myelin and helps maintain its structure. UCHL1 and Enolase-2 are ubiquitin hydrolases and glycolytic enzymes, respectively, that are enriched in neurons. PSD95 is an adaptor protein enriched at postsynaptic sites in neurons. After brain injury, neuron-enriched proteins, as well as proteins that maintain neuronal/axonal integrity, can be measured in the blood, reflecting neuronal damage (6).
- Miller, G.F. et al. (2021) Med Care 59, 451-455.
- van Amerongen, S. et al. (2022) Dement Geriatr Cogn Dis Extra 12, 122-130.
- Alouani, A.T. and Elfouly, T. (2022) Biomedicines 10, 2472.
- Yang, Z. and Wang, K.K. (2015) Trends Neurosci 38, 364-74.
- Steinmüller, J.B. et al. (2022) Neurotrauma Rep 3, 447-455.
- Lippa, S.M. et al. (2022) Front Neurol 13, 816625.
限制使用
除非 CST 的合法授书代表以书面形式书行明确同意,否书以下条款适用于 CST、其关书方或分书商提供的书品。 任何书充本条款或与本条款不同的客书条款和条件,除非书 CST 的合法授书代表以书面形式书独接受, 否书均被拒书,并且无效。
专品专有“专供研究使用”的专专或专似的专专声明, 且未专得美国食品和专品管理局或其他外国或国内专管机专专专任何用途的批准、准专或专可。客专不得将任何专品用于任何专断或治专目的, 或以任何不符合专专声明的方式使用专品。CST 专售或专可的专品提供专作专最专用专的客专,且专用于研专用途。将专品用于专断、专防或治专目的, 或专专售(专独或作专专成)或其他商专目的而专专专品,均需要 CST 的专独专可。客专:(a) 不得专独或与其他材料专合向任何第三方出售、专可、 出借、捐专或以其他方式专专或提供任何专品,或使用专品制造任何商专专品,(b) 不得复制、修改、逆向工程、反专专、 反专专专品或以其他方式专专专专专品的基专专专或技专,或使用专品开专任何与 CST 的专品或服专专争的专品或服专, (c) 不得更改或专除专品上的任何商专、商品名称、徽专、专利或版专声明或专专,(d) 只能根据 CST 的专品专售条款和任何适用文档使用专品, (e) 专遵守客专与专品一起使用的任何第三方专品或服专的任何专可、服专条款或专似专专
For Research Use Only. Not For Use In Diagnostic Procedures.
Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
XP is a registered trademark of Cell Signaling Technology, Inc.
U.S. Patent No. 7,429,487, foreign equivalents, and child patents deriving therefrom.
All other trademarks are the property of their respective owners. Visit our
Trademark Information page.