Thermo Fisher Scientific EML1 Monoclonal Antibody (5G3)

Applications

Western Blot (WB)

• Tested Dilution: 1:500–1:1,000

ELISA

• Tested Concentration: 10 µg/mL

Product Specifications

Product Specific Information

Sequence of this protein is as follows:
MEDGFSSYSS LYDTSSLLQF CNDDSASAAS SMEVTDRIAS LEQRVQMQED DIQLLKSALA DVVRRLNITE EQQAVLNRKG PTKARPLMQT LPLRTTVNN

Target Information

Human echinoderm microtubule-associated protein-like (EML1) is a strong candidate for the Usher syndrome type 1A gene.
Usher syndromes (USHs) are genetic disorders involving congenital deafness, retinitis pigmentosa, and vestibular dysfunction.
They are categorized into:

• Type I (USH1A–USH1F): Most severe form
• Type II (USH2A, USH2B)
• Type III (USH3)

Two transcript variants encoding different isoforms have been found for this gene.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.