Aldolase C Antibody (1A1) [Allophycocyanin/Cy7]

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Product Details

Summary
Product Discontinued
View other related Aldolase C Primary Antibodies

Order Details


    • Catalog Number
      NBP2-25144APCCY7
    • Availability
      Product Discontinued

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Aldolase C Antibody (1A1) [Allophycocyanin/Cy7] Summary

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
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Applications/Dilutions

Dilutions
  • Flow Cytometry
Application Notes
Optimal dilution of this antibody should be experimentally determined. For optimal results using our Tandem dyes, please avoid prolonged exposure to light or extreme temperature fluctuations. These can lead to irreversible degradation or decoupling. When staining intracellular targets, specific attention to the fixation and permeabilization steps in your flow protocol may be required. Please contact our technical support team at technical@novusbio.com if you have any questions.

Packaging, Storage & Formulations

Storage
Store at 4C in the dark. Do not freeze.
Buffer
PBS
Preservative
0.05% Sodium Azide
Purity
Immunogen affinity purified

Alternate Names for Aldolase C Antibody (1A1) [Allophycocyanin/Cy7]

  • ALDC
  • aldolase 3
  • aldolase C, fructose-bisphosphate
  • Brain-type aldolase
  • EC 4.1.2.13
  • fructoaldolase C
  • fructose-1,6-biphosphate triosephosphate lyase
  • fructose-bisphosphate aldolase C

Background

The Aldolase C gene encodes a member of the class I fructose-biphosphate aldolase gene family. Expressed specifically in thehippocampus and Purkinje cells of the brain, the encoded protein is a glycolytic enzyme that catalyzes the reversiblealdol cleavage of fructo

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Secondary Antibodies

 

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Blogs on Aldolase C.

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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Bioinformatics

Gene Symbol ALDOC