SMNDC1 Antibody
Product Specifications
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.
NCBI Gene ID
10285
Swiss Prot
O75940
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-238 of human SMNDC1 (NP_005862.1) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Apoptosis, Cell Cycle
Purification
Affinity purification
Positive Control
HeLa
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 27kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
SMNDC1
Positive Control 2
Jurkat
Positive Control 3
HT-1080
Positive Control 4
PC-12
Positive Control 5
SH-SY5Y
Positive Control 6
SKOV3
NCBI Official Name
Survival motor neuron domain containing 1
NCBI Organism
Homo sapiens
Other Product Names
SMNDC1, SMNR, SPF30, TDRD16C
Tested Applications
WB
Physical Properties
Liquid
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