FLNB anticorps (AA 1551-1650) (HRP)
Aperçu rapide pour FLNB anticorps (AA 1551-1650) (HRP) (ABIN1712051)
Antigène
Voir toutes FLNB AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 1551-1650
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Réactivité croisée
- Humain
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Homologie
- Mouse,Rat,Dog,Cow,Sheep,Rabbit
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Purification
- Purified by Protein A.
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Immunogène
- KLH conjugated synthetic peptide derived from human FLNB/Filamin 3
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Isotype
- IgG
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Indications d'application
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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Agent conservateur
- ProClin
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Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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Conseil sur la manipulation
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
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Stock
- -20 °C
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Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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Date de péremption
- 12 months
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- FLNB (Filamin B, beta (FLNB))
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Autre désignation
- FLNB/Filamin 3
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Sujet
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Synonyms: ABP 278, ABP 280 homolog, ABP-278, ABP-280 homolog, ABP278, Actin binding like protein, Actin binding protein 278, Actin-binding-like protein, AOI, Beta filamin, Beta-filamin, DKFZp686A1668, DKFZp686O033, Fh1, Filamin 1 actin binding protein 280 like, Filamin 3, Filamin B, Filamin B beta actin binding protein 278, Filamin homolog 1, Filamin-3, Filamin-B, FLN B, FLN-B, FLN1L, FLN3, FLNB, FLNB_HUMAN, LRS1, SCT, TABP, TAP, Thyroid autoantigen, Truncated ABP, Truncated actin binding protein, Truncated actin-binding protein.
Background: This gene encodes a member of the filamin family. The encoded protein interacts with glycoprotein Ib alpha as part of the process to repair vascular injuries. The platelet glycoprotein Ib complex includes glycoprotein Ib alpha, and it binds the actin cytoskeleton. Mutations in this gene have been found in several conditions: atelosteogenesis type 1 and type 3, boomerang dysplasia, autosomal dominant Larsen syndrome, and spondylocarpotarsal synostosis syndrome. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Nov 2009].
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ID gène
- 2317
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Pathways
- Maintenance of Protein Location
Antigène
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