SMNDC1 Antilichaam

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.

10285

O75940

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-238 of human SMNDC1 (NP_005862.1) .

Unconjugated

Primary Antibodies

Apoptosis, Cell Cycle

Affinity purification

HeLa

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 27kDa

IgG

WB: 1:500 - 1:2000

SMNDC1

Jurkat

HT-1080

PC-12

SH-SY5Y

SKOV3

Survival motor neuron domain containing 1

Homo sapiens

SMNDC1, SMNR, SPF30, TDRD16C

WB

Liquid