Adamts2 anticorps
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- Antigène Voir toutes Adamts2 Anticorps
- Adamts2 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 2 (Adamts2))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp Adamts2 est non-conjugé
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Application
- Western Blotting (WB)
- Attributs du produit
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogène
- Recombinant protein of mouse ADAMTS2
- Isotype
- IgG
- Top Product
- Discover our top product Adamts2 Anticorps primaire
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- Indications d'application
- WB 1:500-1:2000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- Adamts2 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 2 (Adamts2))
- Autre désignation
- ADAMTS2 (Adamts2 Produits)
- Synonymes
- anticorps ADAM-TS2, anticorps ADAMTS-2, anticorps ADAMTS-3, anticorps PCINP, anticorps hPCPNI, anticorps mKIAA4060, anticorps pNPI, anticorps NPI, anticorps PC I-NP, anticorps PCI-NP, anticorps PCPNI, anticorps PNPI, anticorps RGD1565950, anticorps a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 2, anticorps ADAM metallopeptidase with thrombospondin type 1 motif 2, anticorps ADAM metallopeptidase with thrombospondin type 1 motif, 2, anticorps Adamts2, anticorps ADAMTS2
- Sujet
- This gene 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 encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed.
- Poids moléculaire
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Observed_MW: 120 kDa
Calculated_MW: 61 kDa/134 kDa
- ID gène
- 216725
- UniProt
- Q8C9W3
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