兔抗NIPA1多克隆抗体

Background:

This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6.

Applications:

ELISA, IHC

Name of antibody:

NIPA1

Immunogen:

Full length fusion protein

Full name:

non imprinted in Prader-Willi/Angelman syndrome 1

Synonyms：

FSP3; SPG6

SwissProt:

Q7RTP0

ELISA Recommended dilution:

5000-10000

IHC positive control:

Human brain

IHC Recommend dilution:

25-100