C16orf57 Protein (Myc-DYKDDDDK Tag)
USB1
Origin: Human
Host: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
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- Target See all C16orf57 (USB1) Proteins
- C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This C16orf57 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human C16orf57 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product USB1 Protein
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U6 SnRNA Biogenesis 1 (USB1) (AA 1-265) protein (Strep Tag)
Crystallography grade USB1 Origin: Human Host: Tobacco (Nicotiana tabacum) Recombinant >80 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. ELISA, WB, SDS
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Target
- C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))
- Alternative Name
- c16orf57 (USB1 Products)
- Synonyms
- C16orf57 Protein, HVSL1 Protein, Mpn1 Protein, PN Protein, hUsb1 Protein, C18H16orf57 Protein, AA960436 Protein, RGD1305215 Protein, c16orf57 Protein, C2H16orf57 Protein, zgc:91896 Protein, U6 snRNA biogenesis phosphodiesterase 1 Protein, U6 snRNA biogenesis 1 Protein, U6 snRNA biogenesis phosphodiesterase 1 L homeolog Protein, USB1 Protein, Usb1 Protein, usb1.L Protein, usb1 Protein
- Background
- This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.
- Molecular Weight
- 30.1 kDa
- NCBI Accession
- NP_078874
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