PMP22 Mouse Monoclonal Antibody [Kloon ID: LBI5D1]

This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

Carrier-free (BSA/glycerol-free) PMP22 mouse monoclonal antibody, clone LBI5D1

CMT1A; CMT1E; DSS; GAS-3; GAS3; HMSNIA; HNPP; Sp110

Homo sapiens peripheral myelin protein 22 (PMP22), transcript variant 1, mRNA.

5376

Q01453

Unconjugated

WB 1:500, IHC 1:2000

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Transmembrane

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

PMP22

https://www.ncbi.nlm.nih.gov/gene/?term=5376

https://www.uniprot.org/uniprot/Q01453