兔抗SMNDC1多克隆抗体

Background:

This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene.

Applications:

ELISA, IHC

Name of antibody:

SMNDC1

Immunogen:

Fusion protein of human SMNDC1

Full name:

survival motor neuron domain containing 1

Synonyms:

SMNR; SPF30; TDRD16C

SwissProt:

O75940

ELISA Recommended dilution:

5000-10000

IHC positive control:

Human ovarian cancer

IHC Recommend dilution:

40-200