TJP2 anticorps
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- Antigène Voir toutes TJP2 Anticorps
- TJP2 (Tight Junction Protein 2 (Zona Occludens 2) (TJP2))
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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 TJP2 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC)
- Purification
- Affinity purification
- Immunogène
- Recombinant protein of human TJP2
- Isotype
- IgG
- Top Product
- Discover our top product TJP2 Anticorps primaire
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- Indications d'application
- WB 1:500 - 1:2000 IHC 1:50 - 1:200
- Restrictions
- For Research Use only
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- Concentration
- 1 mg/mL
- Buffer
- 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
- TJP2 (Tight Junction Protein 2 (Zona Occludens 2) (TJP2))
- Autre désignation
- TJP2 (TJP2 Produits)
- Synonymes
- anticorps C9DUPq21.11, anticorps DFNA51, anticorps DUP9q21.11, anticorps X104, anticorps ZO2, anticorps ZO-2, anticorps zo2, anticorps tjp2, anticorps x104, anticorps zo-2, anticorps wu:fb62b09, anticorps zgc:92094, anticorps tight junction protein 2, anticorps tight junction protein 2 L homeolog, anticorps tight junction protein 2b (zona occludens 2), anticorps TJP2, anticorps Tjp2, anticorps tjp2.L, anticorps tjp2b
- Sujet
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Synonyms: C9DUPq21.11,DFNA51,DUP9q21.11,Friedreich ataxia region gene X104 (tight junction protein ZO-2),MGC26306 ,PFIC4,Tight junction protein 2,Tight junction protein ZO 2,Tight junction protein ZO-2,TJP2,X104,ZO 2,ZO-2,ZO2,ZO2,Zona occludens 2,Zona occludens protein 2,Zonula occludens protein 2
Background: This gene encodes a zonula occluden that is a member of the membrane-associated guanylate kinase homolog family. The encoded protein functions as a component of the tight junction barrier in epithelial and endothelial cells and is necessary for proper assembly of tight junctions. Mutations in this gene have been identified in patients with hypercholanemia, and genomic duplication of a 270 kb region including this gene causes autosomal dominant deafness-51. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene.
- Poids moléculaire
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Observed_MW: 160kDa
Calculated_MW: 111-137kDa
- ID gène
- 9414
- UniProt
- Q9UDY2
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