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Superoxide Dismutase 1 (SOD1) Mouse Monoclonal Antibody [Clone ID: LBI8B10]

Superoxide Dismutase 1 (SOD1) Mouse Monoclonal Antibody [Clone ID: LBI8B10]

Item no.	LBI-AMM09166VCF
Manufacturer	Leading Biology
Amount	100 ug
Category	Neuroscience Metabolism Diabetes Molecular Targets for Neuroscience Aging & Neurological Disorders Antibodies Cell Biology Cell Status Cell Metabolism Oxidative Stress
Type	Antibody Monoclonal
Format	Lyophilized
Clone	LBI8B10
Specific against	Human (Homo sapiens)
Host	Mouse
Isotype	IgG2b
Conjugate/Tag	Unconjugated
ECLASS 10.1	42030590
ECLASS 11.0	42030590
UNSPSC	12352203
Alias	ALS, ALS1, HEL-S-44, homodimer, hSod1, IPOA, SOD
Available
Manufacturer - Category	mAbs-V
Manufacturer - Targets	SOD1
Storage Conditions	Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
Field of Research	Amyotrophic lateral sclerosis (ALS), Huntington's disease, Prion diseases
Overview	Carrier-free (BSA/glycerol-free) SOD1 mouse monoclonal antibody, clone LBI8B10
Immunogen	Full length human recombinant protein of human SOD1 (NP_000445) produced in HEK293T cell.
Gene Name	Homo sapiens superoxide dismutase 1 (SOD1), mRNA.
Symbol	SOD1
Function	Druggable Genome
Summary	The protein encoded by this gene binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. The encoded isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene. [provided by RefSeq]
Manufacturer - Format	Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Storage Buffer	Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Dilution	WB 1:1000~2000, IHC 1:50, FLOW 1:100
Purification	Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
Pathway	Amyotrophic lateral sclerosis (ALS), Huntington's disease, Prion diseases

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

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Amount: 100 ug

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Delivery expected until 1/15/2026

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