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Fibrillin 1 Recombinant antibody, PBS Only

Fibrillin 1 Uni-rAbTM Recombinant Antibody for WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, ELISA

Conjugate

Unconjugated

CloneNo.

240960G12

Cat no : 83836-4-PBS

Print datasheet

Synonyms

FBN1, MASS, Fibrillin-1, FBN, Asprosin

验证数据展示

  • WB analysis of HeLa using 83836-4-RR (same clone as 83836-4-PBS)

    WB analysis of HeLa using 83836-4-RR (same clone as 83836-4-PBS)

    HeLa cells were subjected to SDS PAGE followed by western blot with 83836-4-RR (Fibrillin 1 antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 83836-4-PBS in a different storage buffer formulation.

  • Affinity and Kinetic Characterization of 83836-4-RR

    Affinity and Kinetic Characterization of 83836-4-RR

    Biolayer interferometry (BLl) kinetic assays of 83836-4-RR against Human Fibrillin 1 were performed. The affinity constant is 51.3 nM.

产品信息

The immunogen of 83836-4-PBS is Fibrillin 1 Fusion Protein expressed in E. coli.

Tested Applications WB, ELISA Application Description
Tested Reactivity human
Immunogen Fibrillin 1 fusion protein Ag30283 种属同源性预测
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Full Name fibrillin 1
Synonyms FBN1, MASS, Fibrillin-1, FBN, Asprosin
Observed Molecular Weight350 kDa
GenBank Accession NumberBC146854
Gene Symbol Fibrillin 1
Gene ID (NCBI) 2200
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purfication
UNIPROT IDP35555
Storage Buffer PBS Only
Storage ConditionsStore at -80°C.
The product is shipped with ice packs. Upon receipt, store it immediately at -80°C

背景介绍

Fibrillin-1 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 Fibrillin-1 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.