TRIOBP anticorps (AA 1079-2365)
Aperçu rapide pour TRIOBP anticorps (AA 1079-2365) (ABIN7825977)
Antigène
Voir toutes TRIOBP AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 1079-2365
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Fonction
- Anti-TRIOBP Antibody
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Réactivité croisée (Details)
- No cross-reactivity with other proteins
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Attributs du produit
- Anti-TRIOBP Antibody (ABIN7825977). Tested in WB, IHC, IF, IP, Flow Cytometry, ELISA applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.
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Purification
- Immunogen affinity purified.
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Immunogène
- E.coli-derived human TRIOBP recombinant protein (Position: H1079-E2365). Human TRIOBP shares 78.1% amino acid (aa) sequence identity with mouse TRIOBP.
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Isotype
- IgG
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Indications d'application
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Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
Immunohistochemistry, 2-5 μg/mL, Human
Immunofluorescence, 5 μg/mL, Human
Immunoprecipitation, 0.5-2 μg/mL, Human
Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
ELISA, 0.1-0.5 μg/mL
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
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At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
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- TRIOBP (TRIO and F-Actin Binding Protein (TRIOBP))
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Autre désignation
- TRIOBP
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Sujet
- This gene encodes a protein with an N-terminal pleckstrin homology domain and a C-terminal coiled-coil region. The protein interacts with trio, which is involved with neural tissue development and controlling actin cytoskeleton organization, cell motility and cell growth. The protein also associates with F-actin and stabilizes F-actin structures. Mutations in this gene have been associated with a form of autosomal recessive nonsyndromic deafness. Multiple alternatively spliced transcript variants that would encode different isoforms have been found for this gene, however some transcripts may be subject to nonsense-mediated decay (NMD).
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Poids moléculaire
- 75 kDa
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ID gène
- 11078
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UniProt
- Q9H2D6
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Pathways
- Regulation of Actin Filament Polymerization
Antigène
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