Traumatic brain injury (TBI) and spinal cord injury (SCI) involve primary mechanical damage followed by secondary injury cascades including neuroinflammation, excitotoxicity, and reactive gliosis. FDA-cleared blood biomarkers (GFAP, UCH-L1) now enable rapid mild TBI triage, while NfL and S100B are emerging as prognostic markers. Research focuses on neuroprotection, axon regeneration, and rehabilitation biomarkers.
Research Use Only (RUO)Not intended for diagnostic or therapeutic procedures.
Fig. 1 Key pathogenic pathways and research targets. abinScience product targets highlighted in orange.
abinScience provides validated antibodies, recombinant proteins, and ELISA kits for key TBI and spinal cord injury research targets. All products are manufactured by our parent company AtaGenix Laboratories under ISO quality systems. Browse products below or contact us for custom antibody development.
GFAP — Serum GFAP is an FDA-cleared biomarker for mild TBI evaluation (Banyan Brain Trauma Indicator). Anti-GFAP antibodies support point-of-care assay development and astrocyte damage quantification in neurotrauma research.
→ Browse GFAP antibodies & ELISA kits
UCH-L1 — UCH-L1 (ubiquitin C-terminal hydrolase L1) is released from damaged neurons and is an FDA-cleared TBI biomarker paired with GFAP. Anti-UCH-L1 antibodies enable neuronal injury detection in serum and CSF.
→ Browse UCH-L1 antibodies & proteins
NfL (Neurofilament Light Chain) — Serum NfL reflects axonal damage severity in TBI and SCI, correlating with injury severity and long-term outcomes. Anti-NfL antibodies support prognostic assay development and rehabilitation monitoring.
1. Maas AIR, et al. Traumatic brain injury: integrated approaches to improve prevention, clinical care, and research. Lancet Neurol. 2017;16(12):987-1048. DOI
2. Bazarian JJ, et al. Serum GFAP and UCH-L1 for prediction of absence of intracranial injuries on head CT (ALERT-TBI). Lancet Neurol. 2018;17(9):782-789. DOI
3. Ahadi R, et al. Diagnostic value of serum levels of GFAP, pNF-H, and NSE compared with clinical findings in severity assessment of human traumatic spinal cord injury. Spine. 2015;40(14):E823-830. DOI
Human
ELISA, FCM, FuncS
Human
Monoclonal
IgG1
H27K15
Human
ELISA, Bioactivity: FCM, Functional assay, Research in vivo
Human
Monoclonal
IgG1-nd
Human
ELISA, Bioactivity: FCM, Functional assay, Research in vivo
Human
Monoclonal
IgG4-kappa
Human
ELISA, Bioactivity: FACS, Functional assay, Research in vivo
Human
Monoclonal
IgG4-kappa
Human
ELISA, Bioactivity: FACS, Functional assay, Research in vivo
Human
Monoclonal
IgG1-kappa
Human
ELISA, Bioactivity: FACS, Functional assay, Research in vivo
Human
Monoclonal
IgG4-kappa
Human
ELISA, Bioactivity: FCM, Functional assay, Research in vivo
Human
Monoclonal
IgG4-nd
Human
Blocking, DB, FCM, IHC
Mouse
Monoclonal
IgG1, kappa
mAb107
E. coli
P14136
Leu292-Met432
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)
Mammalian cells
P07333
Met1-Glu512
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)