Anti-EML1 Antilichaam

Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type. The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems. The USHs are catagorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3) . The type I is the most severe form. Gene loci responsible for these three types are all mapped. Two transcript variants encoding different isoforms have been found for this gene.

Boster Bio Anti-EML1 Antibody catalog # A08919-1. Tested in WB, ELISA applications. This antibody reacts with Human, Mouse, Rat.

EML1

O00423

Human, Mouse, Rat

E.coli-derived human EML1 recombinant protein (Position: 3-347) .

WB, ELISA

Immunogen affinity purified.

500 μg/mL

Liquid

12 months from date of receipt, -20°C as supplied. 6 months 2 to 8°C after reconstitution. Avoid repeated freezing and thawing.

https://www.bosterbio.com/msds?sku=A08919-1

500 μg/mL antibody with PBS,0.02% NaN3, 1 mg BSA and 50% glycerol.