GM2A Antibody - BSA Free

Immunohistochemistry-Paraffin: GM2A Antibody [NBP1-44366] - Analysis of anti-GM2A antibody with human kidney.

Immunohistochemistry-Paraffin: GM2A Antibody [NBP1-44366] - Analysis of anti-GM2A antibody with human breast.

• Reactivity: Hu, Pm, Pm-Or, Pm
• Applications: IHC
• Clonality: Polyclonal
• Host: Rabbit
• Conjugate: Unconjugated
• Format: BSA Free
• Concentration: 1.0 mg/ml

GM2A Antibody - BSA Free Summary

• Description: Product can be stored undiluted at 4C for up to 1 month.
• Immunogen: Synthetic 15 amino acid peptide from internal region of human GM2A.
• Epitope: Internal region
• Specificity: Human GM2A. BLAST analysis of the peptide immunogen showed no homology with other human proteins.
• Predicted Species: Chimpanzee (100%), Orangutan (100%), Primate (100%). Backed by our 100% Guarantee.
• Isotype: IgG
• Clonality: Polyclonal
• Host: Rabbit
• Gene: GM2A
• Purity: Immunogen affinity purified

Applications/Dilutions

• Dilutions:
  • Immunohistochemistry
  • Immunohistochemistry-Paraffin 5 ug/ml
• Application Notes: .

Reactivity Notes

Predicted cross-reactivity based on sequence identity: Gorilla (100%), Gibbon (100%), Marmoset (93%).

Packaging, Storage & Formulations

• Storage: Keep as concentrated solution. Aliquot and store at -20C or below. Avoid multiple freeze-thaw cycles.
• Buffer: PBS
• Preservative: 0.1% Sodium Azide
• Concentration: 1.0 mg/ml
• Purity: Immunogen affinity purified

Alternate Names for GM2A Antibody - BSA Free

• Cerebroside sulfate activator protein
• ganglioside GM2 activator
• GM2 ganglioside activator
• GM2-AP
• SAP-3GM2 ganglioside activator protein
• Shingolipid activator protein 3
• sphingolipid activator protein 3

Background

This gene encodes a small glycolipid transport protein which acts as a substrate specific co-factor for the lysosomal enzyme beta-hexosaminidase A. Beta-hexosaminidase A, together with GM2 ganglioside activator, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene result in GM2-gangliosidosis type AB or the AB variant of Tay-Sachs disease.

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.

Bioinformatics

• Gene Symbol: GM2A