Fibrillin 1 antibody (AA 2780-2860)
Quick Overview for Fibrillin 1 antibody (AA 2780-2860) (ABIN7220476)
Target
See all Fibrillin 1 (FBN1) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 2780-2860
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Purpose
- FBN1 Polyclonal Antibody
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Specificity
- FBN1 Polyclonal Antibody detects endogenous levels of FBN1 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from the C-terminal region of human FBN1 at AA range: 2780-2860
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IHC-P (1:100-1:300), ELISA (1:40000). Not yet tested in other applications.
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Comment
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- Fibrillin 1 (FBN1)
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Alternative Name
- FBN1
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Background
- Rabbit Anti-FBN1 Polyclonal Antibody,FBN1, FBN, Fibrillin-1,FBN1 encodes a member of the fibrillin family of proteins. The encoded preproprotein is proteolytically processed to generate two proteins including the extracellular matrix component fibrillin-1 and the protein hormone asprosin. Fibrillin-1 is an extracellular matrix glycoprotein that serves as a structural component of calcium-binding microfibrils. These microfibrils provide force-bearing structural support in elastic and nonelastic connective tissue throughout the body. Asprosin, secreted by white adipose tissue, has been shown to regulate glucose homeostasis. Mutations in this gene are associated with Marfan syndrome and the related MASS phenotype, as well as ectopia lentis syndrome, Weill-Marchesani syndrome, Shprintzen-Goldberg syndrome and neonatal progeroid syndrome.,Fibrillin-1
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Gene ID
- 2200
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UniProt
- P35555
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Pathways
- Maintenance of Protein Location, SARS-CoV-2 Protein Interactome
Target
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