Reactivity | Hu, Rt, Bv, Ca, Mu(-)Species Glossary |
Applications | WB, Flow, ICC/IF, CyTOF-ready |
Clone | 1A1 |
Clonality | Monoclonal |
Host | Mouse |
Conjugate | Unconjugated |
Format | BSA Free |
Concentration | 1 mg/ml |
Description | Novus Biologicals Mouse Aldolase C Antibody (1A1) - BSA Free (NBP2-25144) is a monoclonal antibody validated for use in WB, Flow and ICC/IF. All Novus Biologicals antibodies are covered by our 100% guarantee. |
Immunogen | The C-terminal 23 amino acids of human Aldolase C (KYEGSGEDGGAAAQSLYIANHAY). [UniProt# P09972] |
Marker | pan-Astrocyte Marker |
Isotype | IgG1 |
Clonality | Monoclonal |
Host | Mouse |
Gene | ALDOC |
Purity | Immunogen affinity purified |
Innovator's Reward | Test in a species/application not listed above to receive a full credit towards a future purchase. |
Dilutions |
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Application Notes | This Aldolase C (1A1) antibody is useful for Immunocytochemistry/Immunofluorescence and Western Blot, where a band can be seen at ~40 kDa. The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. This antibody is CyTOF ready. |
Theoretical MW | 40 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
Storage | Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles. |
Buffer | 50% PBS, 50% glycerol |
Preservative | 5mM Sodium Azide |
Concentration | 1 mg/ml |
Purity | Immunogen affinity purified |
Secondary Antibodies |
Isotype Controls |
Research Areas for Aldolase C Antibody (NBP2-25144)Find related products by research area.
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RNA-binding protein Staufen1 conspires with Atxn2 in stress granules to cause neurodegeneration by dysregulating RNA metabolism By Jamshed Arslan Pharm.D. Spinocerebellar ataxia type 2 (SCA2) is a movement disorder characterized by neurodegeneration. The cause of this autosomal dominant disease is a mutation in the RNA processing gene Atxn2,... Read full blog post. |
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