FBN1-Specific Polyclonal antibody
FBN1-Specific Polyclonal Antibody for IHC,ELISA
Host / Isotype
Rabbit / IgG
Reactivity
human, mouse, rat
Applications
IHC,ELISA
Conjugate
Unconjugated
验证数据展示
产品信息
20251-1-AP targets FBN1-Specific in IHC, ELISA applications and shows reactivity with human, mouse, rat samples.
| Tested Applications | IHC,ELISA |
| Tested Reactivity | human, mouse, rat |
| Immunogen | Peptide 种属同源性预测 |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Full Name | fibrillin 1 |
| Synonyms | FBN, FBN1, fibrillin 1, MASS, MFS1, OCTD, SGS, WMS |
| Calculated Molecular Weight | 312 kDa |
| GenBank Accession Number | NM_000138 |
| Gene Symbol | FBN1 |
| Gene ID (NCBI) | 2200 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification Method | Antigen affinity purification |
| UNIPROT ID | P35555 |
| Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
| Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
FBN1, also named as FBN, belongs to the fibrillin family. Fibrillins are structural components of 10-12 nm extracellular calcium-binding microfibrils, which occur either in association with elastin or in elastin-free bundles. Fibrillin-1-containing microfibrils provide long-term force bearing structural support. Defects in FBN1 are a cause of Marfan syndrome (MFS), isolated ectopia lentis (EL), Weill-Marchesani syndrome autosomal dominant (ADWMS), Shprintzen-Goldberg craniosynostosis syndrome (SGS) or MASS syndrome. This antibody is specific to FBN1.
