13 Results for "

neurofilament light chain

" in MedChemExpress (MCE) Product Catalog:
Products (13)

13 Results for "neurofilament light chain" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-132580
CAS No.: 2088232-70-4
Purity:  96.53%
Synonyms: BIIB067; ISIS-SOD1Rx; ISIS 333611
Target:  

SOD

Research Areas:  

Neurological Disease

Tofersen (BIIB067) is an antisense oligonucleotide and SOD1 mRNA inhibitor with an IC50 of 320 pM. Tofersen mediates RNase H-dependent degradation of SOD1 mRNA to reduce SOD1 protein levels in cerebrospinal fluid and serum. Tofersen downregulates cerebrospinal fluid neurofilament light chain, neurofilament heavy chain, amyloid-beta 1-40, amyloid-beta 1-42, neuropeptide Y, ubiquitin C-terminal hydrolase L1, neuropentraxins 1, 2, R, corticotropin-releasing hormone, IL-15, and serum neurofilament light chain, neurofilament heavy chain. Tofersen can be used for the research of superoxide dismutase 1-associated amyotrophic lateral sclerosis .
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2
2 Cited Publications
Cat. No.: HY-132580A
CAS No.: 1898254-60-8
Purity:  97.19%
Synonyms: BIIB067 sodium; ISIS-SOD1Rx sodium; ISIS 333611 sodium
Target:  

SOD

Research Areas:  

Neurological Disease

Tofersen (BIIB067) sodium is an antisense oligonucleotide and SOD1 mRNA inhibitor with an IC50 of 320 pM. Tofersen sodium mediates RNase H-dependent degradation of SOD1 mRNA to reduce SOD1 protein levels in cerebrospinal fluid and serum. Tofersen sodium downregulates cerebrospinal fluid neurofilament light chain, neurofilament heavy chain, amyloid-beta 1-40, amyloid-beta 1-42, neuropeptide Y, ubiquitin C-terminal hydrolase L1, neuropentraxins 1, 2, R, corticotropin-releasing hormone, IL-15, and serum neurofilament light chain, neurofilament heavy chain. Tofersen sodium can be used for the research of superoxide dismutase 1-associated amyotrophic lateral sclerosis .
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Cat. No.: HY-173276
CAS No.: 3069378-18-0
Research Areas:  

Neurological Disease

SARM1-IN-4 (Compound 7) is an orally active SARM1 inhibitor. After being orally administered at a dose of 50 mg/kg in a mouse model, it can reduce the level of plasma neurofilament light chain (NfL). SARM1-IN-4 prevents programmed axonal degeneration by inhibiting the NAD+ hydrolase activity of SARM1, and it can be used in research related to neurodegenerative diseases and neurological disorders (such as multiple sclerosis, amyotrophic lateral sclerosis, Parkinson's disease, and peripheral neuropathies, etc.).
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Cat. No.: HY-W611371
CAS No.: 61694-81-3
Target:  

TRP Channel iGluR

Research Areas:  

Neurological Disease

FP802 is an orally active potent TwinF interface inhibitor that disrupts and detoxifies the NMDAR/TRPM4 death complex. FP802 exerts powerful neuroprotective effects in the 5xFAD mouse model of Alzheimer’s disease (AD) by preventing cognitive decline, preserving neuronal structural integrity, reducing amyloid-β plaque formation, and mitigating mitochondrial pathology . FP802 stops loss of motor neurons, reduces serum neurofilament light chain (NfL) levels, improves motor performance, and extends life in a mouse model of amyotrophic lateral sclerosis (ALS). FP802 can be used for AD and ALS research .
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Cat. No.: HY-132580S
Synonyms: BIIB067-d27; ISIS-SOD1Rx-d27; ISIS 333611-d27
Tofersen-d27 (BIIB067-d27) is the deuterium labeled Tofersen (HY-132580). Tofersen (BIIB067) is an antisense oligonucleotide and SOD1 mRNA inhibitor with an IC50 of 320 pM. Tofersen mediates RNase H-dependent degradation of SOD1 mRNA to reduce SOD1 protein levels in cerebrospinal fluid and serum. Tofersen downregulates cerebrospinal fluid neurofilament light chain, neurofilament heavy chain, amyloid-beta 1-40, amyloid-beta 1-42, neuropeptide Y, ubiquitin C-terminal hydrolase L1, neuropentraxins 1, 2, R, corticotropin-releasing hormone, IL-15, and serum neurofilament light chain, neurofilament heavy chain. Tofersen can be used for the research of superoxide dismutase 1-associated amyotrophic lateral sclerosis.
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Cat. No.: HY-W611371A
CAS No.: 2490401-57-3
Target:  

TRP Channel iGluR

Research Areas:  

Neurological Disease

FP802 dihydrochloride is an orally active potent TwinF interface inhibitor that disrupts and detoxifies the NMDAR/TRPM4 death complex. FP802 dihydrochloride exerts powerful neuroprotective effects in the 5xFAD mouse model of Alzheimer’s disease (AD) by preventing cognitive decline, preserving neuronal structural integrity, reducing amyloid-β plaque formation, and mitigating mitochondrial pathology . FP802 dihydrochloride stops loss of motor neurons, reduces serum neurofilament light chain (NfL) levels, improves motor performance, and extends life in a mouse model of amyotrophic lateral sclerosis (ALS) . FP802 dihydrochloride can be used for AD and ALS research .
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Cat. No.: HY-P706271
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ¹⁵N-NF-L; ¹⁵N-neurofilament 68; ¹⁵N-neurofilament triplet L; ¹⁵N-70 kD neurofilament light; ¹⁵N-68kDa neurofilament protein; ¹⁵N-CMT 1F; ¹⁵N-CMT 2E; ¹⁵N-FLJ53642; ¹⁵N-NEFL; ¹⁵N-neurofilament light polypeptide; NEFL; light Molecular Weight neurofilament Protein; neurofilament light chain; neurofilament light Polypeptide Isoform 1; NF68; neurofilament light Polypeptide Isoform 2; NFL; neurofilament Protein; light chain; PPP1R110; neurofilament; light Polypeptide; CMT1F; 68 KDa neurofilament Protein; CMT2E; neurofilament Subunit NF-L; Protein Phosphatase 1; Regulatory Subunit 110; neurofilament light; neurofilament; light Polypeptide 68kDa; neurofilament-light; neurofilament light Polypeptide; NEFL Protein; neurofilament Triplet L Protein; CMTDIG; NF-L
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P704813
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: NEFL; light Molecular Weight neurofilament Protein; neurofilament light chain; neurofilament light Polypeptide Isoform 1; NF68; neurofilament light Polypeptide Isoform 2; NFL; neurofilament Protein, light chain; PPP1R110; neurofilament, light Polypeptide
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P72265
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: NEFL; light Molecular Weight neurofilament Protein; neurofilament light chain; neurofilament light Polypeptide Isoform 1; NF68; neurofilament light Polypeptide Isoform 2; NFL; neurofilament Protein, light chain; PPP1R110; neurofilament, light Polypeptide
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P72305
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: NEFL; light Molecular Weight neurofilament Protein; neurofilament light chain; neurofilament light Polypeptide Isoform 1; NF68; neurofilament light Polypeptide Isoform 2; NFL; neurofilament Protein, light chain; PPP1R110; neurofilament, light Polypeptide; CMT1F; 68 KDa neurofilament Protein; CMT2E; neurofilament Subunit NF-L; Protein Phosphatase 1, Regulatory Subunit 110; neurofilament light; neurofilament, light Polypeptide 68kDa; neurofilament-light; neurofilament light Polypeptide; NEFL Protein; neurofilament Triplet L Protein; CMTDIG; NF-L
Species:  
Mouse
Source:  
E. coli
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Cat. No.: HY-P86702
Synonyms: neurofilament L; neurofilament 68; neurofilament triplet L; 70 kD neurofilament light; 68kDa neurofilament protein; CMT 1F; CMT 2E; CMT1F; CMT2E; FLJ53642; light molecular weight neurofilament protein; NEFL; neurofilament light; neurofilament light polypeptide 68kDa; neurofilament light polypeptide; neurofilament protein, light chain; neurofilament subunit NF L; neurofilament triplet L protein; NF 68; NF L; NF68; NFL; NFL_HUMAN.

Host:  

Rabbit

Application:  

WB, IHC-P, IHC-F, IF-Tissue

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-187302S
[U- 15N]-NfL is the 15N-labeled NfL. Neurofilament light chain (NfL) is a major component of neuronal axonal intermediate filaments and serves as a specific marker of neuronal injury in conditions such as neurodegenerative diseases and traumatic brain injury. This isotope can be used in NMR studies to investigate disease mechanisms and in mass spectrometry analysis.
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Cat. No.: HY-P992512
Target:  

Complement System

Research Areas:  

Neurological Disease

ANX-M1 Mouse IgG1 is a brain-penetrant C1q inhibitor. ANX-M1 Mouse IgG1 blocks classical complement pathway activation, reduces C1q concentrations in brain and plasma, and inhibits microglia-mediated synapse engulfment. ANX-M1 Mouse IgG1 can be used for the research of Huntington's disease, Alzheimer's disease, retinopathy and neuropathic pain .
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