C16orf57 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2715417

Détail du produit

Antigène: C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette C16orf57 protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human C16orf57 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: 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.

Détail du antigène

Antigène: C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Autre désignation: c16orf57 (USB1 Produits)

Synonymes: 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

Sujet: 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.

Poids moléculaire: 30.1 kDa

NCBI Accession: NP_078874