SMNDC1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5102320-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5102320 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
SMNDC1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
SMNDC1
Gene Alias
2410004J23Rik; 30 kDa splicing factor SMNrp; 4933440I19Rik; MGC106917; MGC112663; SMN related protein; SMNDC1; SMNR; SMN-related protein; Spf30; splicing factor 30, survival of motor neuron-related; survival motor neuron domain containing 1; survival motor neuron domain-containing protein 1; Survival of motor neuron-related-splicing factor 30; TDRD10; TDRD16C; tudor domain containing 16C; wu:fb37h07; wu:fc23a07
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
10285, 287768, 76479
Content And Storage
-20°C
Form
Liquid
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Gene Accession No.
O75940, Q4QQU6, Q8BGT7
Gene Symbols
SMNDC1
Immunogen
A synthesized peptide derived from human SMNDC1(Accession O75940), corresponding to amino acid residues L45-E95.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Non-human Primate, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Antibody detects endogenous levels of total SMNDC1
- 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.