Survival Motor Neuron Domain Containing 1 (SMNDC1) Peptide
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- Target See all SMNDC1 products
- SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
- Peptide Type
- Synthetic
- Origin
- Mammalian
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Sequence
- KGQVKRSIFA SPESVTGKVG VGTCGIADKP MTQYQDTSKY NVRHLMPQ
- Characteristics
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A synthetic peptide for use as a blocking control in assays to test for specificity of SMNDC1 antibody,
Alternative Names: SMNDC1 control peptide, SMNDC1 antibody Blocking Peptide, Anti-SMNDC1 Blocking Peptide, Survival Motor Neuron Domain Containing 1 Blocking Peptide, SMNR Blocking Peptide, SPF30 Blocking Peptide, SMNDC1, SMNDC-1, SMNDC 1, SMNDC-1 Blocking Peptide, SMNDC 1 Blocking Peptide
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- Application Notes
- Optimal conditions should be determined by the investigator
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- Buffer
- PBS
- Handling Advice
- Avoid repeated freeze/thaw cycles.
- Storage
- -20 °C
- Storage Comment
- Store at -20 °C long term.
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- Target
- SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
- 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. SMNDC1 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. 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.
- Molecular Weight
- 27 kDa
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