ADAMTS2 Antibody - BSA Free

Immunocytochemistry/Immunofluorescence: ADAMTS2 Antibody [NBP3-17208] - Staining of human cell line ASC TERT1 shows localization to plasma membrane.

• Reactivity: Hu
• Applications: ICC/IF
• Clonality: Polyclonal
• Host: Rabbit
• Conjugate: Unconjugated
• Format: BSA Free

ADAMTS2 Antibody - BSA Free Summary

• Immunogen: This antibody was developed against Recombinant Protein corresponding to amino acids: IEPLEKGLAAQEAEQGRVHVVYRRPPTSPPLGGPQALDTGASLDSLDSLSRALGVLEEHANSSRRRARRHAADDDYNIEV
• Isotype: IgG
• Clonality: Polyclonal
• Host: Rabbit
• Gene: ADAMTS2
• Purity: Affinity purified

Applications/Dilutions

• Dilutions:
  • Immunocytochemistry/ Immunofluorescence 0.25-2 ug/ml
• Application Notes: Immunocytochemistry/Immunofluorescence, PFA/Triton X-100 is recommended for fixation/permeabilization.

Packaging, Storage & Formulations

• Storage: Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
• Buffer: PBS, pH 7.2, 40% glycerol
• Preservative: 0.02% Sodium Azide
• Purity: Affinity purified

Alternate Names for ADAMTS2 Antibody - BSA Free

• A disintegrin and metalloproteinase with thrombospondin motifs 2
• a disintegrin-like and metalloprotease (reprolysin type) with thrombospondintype 1 motif, 2
• ADAM metallopeptidase with thrombospondin type 1 motif, 2
• ADAM-TS 2
• ADAMTS2
• ADAMTS-2
• ADAM-TS2EC 3.4.24.14
• ADAMTS-3
• EC 3.4.24
• EDSDERMS
• HPCPNI
• NPIDKFZp686F12218
• PC I-NP
• PCINP
• PCI-NP
• PCINPhPCPNI
• PCPNI
• PNPI
• Procollagen I N-proteinase
• Procollagen I/II amino propeptide-processing enzyme
• Procollagen N-endopeptidase

Background

ADAMTS2 encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The enzyme encoded by this gene excises the N-propeptide of type I, type II and type V procollagens. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in two transcript variants. The short transcript encodes a protein which has no significant procollagen N-peptidase activity.

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: ADAMTS2