ADAMTS2 Antibody - BSA Free

Western Blot: ADAMTS2 Antibody [NBP2-84393] - Host: Rabbit. Target Name: ADAMTS2. Sample Tissue: Human HT1080 Whole Cell lysates. Antibody Dilution: 1ug/ml

• Reactivity: Hu
• Applications: WB
• Clonality: Polyclonal
• Host: Rabbit
• Conjugate: Unconjugated
• Format: BSA Free
• Concentration: 0.5 mg/ml

ADAMTS2 Antibody - BSA Free Summary

• Immunogen: The immunogen is a synthetic peptide directed towards the middle terminal region of human ADAMTS2. Peptide sequence: EHANSSRRRARRHAADDDYNIEVLLGVDDSVVQFHGKEHVQKYLLTLMNI The peptide sequence for this immunogen was taken from within the described region.
• Clonality: Polyclonal
• Host: Rabbit
• Gene: ADAMTS2
• Purity: Affinity purified

Applications/Dilutions

• Dilutions:
  • Western Blot 1.0 ug/ml

Packaging, Storage & Formulations

• Storage: Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
• Buffer: PBS, 2% Sucrose
• Preservative: 0.09% Sodium Azide
• Concentration: 0.5 mg/ml
• 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