Fascin 2 anticorps (AA 1-167)
Aperçu rapide pour Fascin 2 anticorps (AA 1-167) (ABIN7599023)
Antigène
Voir toutes Fascin 2 (FSCN2) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 1-167
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Fonction
- Anti-Fascin 2/FSCN2 Antibody
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Réactivité croisée (Details)
- No cross-reactivity with other proteins.
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Attributs du produit
- Anti-Fascin 2/FSCN2 Antibody (ABIN7599023). Tested in ELISA, WB 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 Fascin 2/FSCN2 recombinant protein (Position: M1-K167).
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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
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
- Add 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, 0.05 mg Sodium azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
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Store 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 freeze-thaw cycles.
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- Fascin 2 (FSCN2)
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Autre désignation
- FSCN2
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Sujet
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Synonyms: Fascin-2, Retinal fascin, FSCN2
Tissue Specificity: Localized specifically in the outer and inner segments of the photoreceptor cells in the retina.
Background: Fascin-2 is a protein that in humans is encoded by the FSCN2 gene. It is mapped to 17q25.3. This gene encodes a member of the fascin protein family. Fascins crosslink actin into filamentous bundles within dynamic cell extensions. This family member is proposed to play a role in photoreceptor disk morphogenesis. A mutation in this gene results in one form of autosomal dominant retinitis pigmentosa and macular degeneration. Multiple transcript variants encoding different isoforms have been found for this gene.
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Poids moléculaire
- 60 kDa
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ID gène
- 25794
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UniProt
- O14926
Antigène
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