Fibrillin 1 anticorps (C-Term)
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- Antigène Voir toutes Fibrillin 1 (FBN1) Anticorps
- Fibrillin 1 (FBN1)
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Épitope
- C-Term
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp Fibrillin 1 est non-conjugé
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Application
- Western Blotting (WB)
- Réactivité croisée
- Humain
- Attributs du produit
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Rabbit Polyclonal antibody to Fibrillin 1 (fibrillin 1)
Fibrillin 1 antibody [C3], C-term - Purification
- Affinity purified by Protein A.
- Immunogène
- Recombinant protein encompassing a sequence within the C-terminus region of human Fibrillin 1. The exact sequence is proprietary.
- Isotype
- IgG
- Top Product
- Discover our top product FBN1 Anticorps primaire
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- Indications d'application
- WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- Commentaires
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Positive Control: HeLa
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 2 mg/mL
- Buffer
- 1XPBS ( pH 7), 40 % Glycerol, 0.01 % Thimerosal
- Agent conservateur
- Thimerosal (Merthiolate)
- Précaution d'utilisation
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- Antigène
- Fibrillin 1 (FBN1)
- Autre désignation
- fibrillin 1 (FBN1 Produits)
- Synonymes
- anticorps FBN1, anticorps ACMICD, anticorps ECTOL1, anticorps FBN, anticorps GPHYSD2, anticorps MASS, anticorps MFS1, anticorps OCTD, anticorps SGS, anticorps SSKS, anticorps WMS, anticorps WMS2, anticorps AI536462, anticorps B430209H23, anticorps Fib-1, anticorps Tsk, anticorps fibrillin 1, anticorps FBN1, anticorps Fbn1
- Sujet
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This gene encodes a member of the fibrillin family. The encoded protein is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated with Marfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.
Cellular Localization: Secreted , extracellular space , extracellular matrix - Poids moléculaire
- 312 kDa
- ID gène
- 2200
- UniProt
- P35555
- Pathways
- Maintenance of Protein Location, SARS-CoV-2 Protein Interactome
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