兔抗MNX1多克隆抗体

Background:

This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Applications:

ELISA, WB

Name of antibody:

MNX1

Immunogen:

Synthetic peptide of human MNX1

Full name:

motor neuron and pancreas homeobox 1

Synonyms:

HB9; HLXB9; SCRA1; HOXHB9

SwissProt:

P50219

ELISA Recommended dilution:

5000-10000

WB Predicted band size:

41 kDa

WB Positive control:

Raji and HepG2 cell lysates

WB Recommended dilution:

200-1000