SMN1 Protein (AA 2-294) (His tag)
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- Target See all SMN1 Proteins
- SMN1 (Survival of Motor Neuron 1, Telomeric (SMN1))
- Protein Type
- Recombinant
- Protein Characteristics
- AA 2-294
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Origin
- Human
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Source
- Escherichia coli (E. coli)
- Purification tag / Conjugate
- This SMN1 protein is labelled with His tag.
- Application
- Western Blotting (WB), SDS-PAGE (SDS), Immunogen (Imm), Positive Control (PC)
- Sequence
- Ala2-Asn294
- Characteristics
- Tag location: N-terminal His-Tag, T7 tag
- Purity
- > 97 %
- Top Product
- Discover our top product SMN1 Protein
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- Application Notes
- Optimal working dilution should be determined by the investigator.
- Comment
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Isoelectric Point:6.2
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Buffer
- 20 mM Tris, 150 mM NaCl, pH 8.0, containing 1 mM EDTA, 1 mM DTT, 0.01 % SKL, 5 % Trehalose and Proclin300.
- Preservative
- ProClin
- Storage
- 4 °C,-80 °C
- Storage Comment
- Store at 2-8°C for one month. Aliquot and store at -80°C for 12 months.
- Expiry Date
- 12 months
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- Target
- SMN1 (Survival of Motor Neuron 1, Telomeric (SMN1))
- Alternative Name
- Survival Motor Neuron Protein (SMN1 Products)
- Synonyms
- SMN2 Protein, Smn Protein, SMN Protein, BCD541 Protein, GEMIN1 Protein, SMA Protein, SMA1 Protein, SMA2 Protein, SMA3 Protein, SMA4 Protein, SMA@ Protein, SMNT Protein, T-BCD541 Protein, TDRD16A Protein, AI849087 Protein, Gemin1 Protein, SMN1 Protein, QtsA-10002 Protein, fa12d01 Protein, smn Protein, wu:fa12d01 Protein, survival motor neuron protein Protein, survival of motor neuron 1, telomeric Protein, survival motor neuron 1 Protein, survival of motor neuron 2, centromeric Protein, survival motor neuron protein-like Protein, survival motor neuron Protein, LOC461829 Protein, Smn1 Protein, SMN1 Protein, SMN2 Protein, LOC100348318 Protein, SMN Protein, LOC100713418 Protein, LOC100065744 Protein, LOC102176643 Protein, smn1 Protein
- Background
- BCD541, SMA1, SMN1, SMA2, SMA3, SMA4, SMNT, T-BCD541, SMNC, Gemin-1, Survival Of Motor Neuron 1, Telomeric, Component of gems 1, Spinal Muscular Atrophy(Werdnig-Hoffmann Disease,Kugelberg-Welander Dis
- Molecular Weight
- 35.4kDa
- UniProt
- Q16637
- Pathways
- Ribonucleoprotein Complex Subunit Organization
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