FBN1 Polyclonal Antibody
| Code | Size | Price |
|---|
| E-AB-12404-20uL | 20uL | £125.00 |
Quantity:
| E-AB-12404-60uL | 60uL | £172.00 |
Quantity:
| E-AB-12404-120uL | 120uL | £237.00 |
Quantity:
| E-AB-12404-200uL | 200uL | £344.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Host Type: Rabbit
Antibody Isotype: IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species:
- Human
- Mouse
Applications:
- Enzyme-Linked Immunosorbent Assay (ELISA)
- Immunohistochemistry (IHC)
Shipping:
Ice packs
Storage:
-20°C
Further Information
Abbreviation:
FBN1
Background:
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 witHuman, Mousearfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.
Buffer:
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration:
0.3 mg/mL
Conjugation:
Unconjugated
Dilution:
IHC 1:50-1:200
Immunogen:
Synthetic peptide of human FBN1
Purification method:
Affinity purification
Target Synonym:
350 kDa glycoprotein component extracellular microfibril;ACMICD;FBN 1;FBN;FBN1;FBN1;Fibrillin 15;Fibrillin-1;Fibrillin1;Fibrillin15;GPHYSD2;Marfan syndrome;MASS;MFS 1;MFS1;OCTD;SGS;SSKS;Weill Marchesani syndrome;WMS;WMS2
UNIProt ID:
P35555