AbPlus™ Anti-TYMS Magnetic Beads (VS-0724-YC961)

CAT#: VS-0724-YC961

The AbPlus Anti-TYMS Magnetic Beads (VS-0724-YC961) is an innovative affinity resin which is bound with anti-TYMS specific antibody. The beads were designed for small-scale affinity purification and immunoprecipitation (IP) of TYMS protein under native and denaturing conditions.

Gene Expression
Figure 1 Tonsil Figure 2 Lymph node Figure 3 Testis Figure 4 Bone marrow Figure 5 RNA cell line category: Low cell line specificity

Specifications

  • Applications
  • Immunoprecipitation, Protein Purification
  • Matrix
  • Magnetic bead
  • Bead Ligand
  • Anti-TYMS specific antibody
  • Target
  • TYMS
  • Immunogen
  • Synthetic peptide corresponding to the C-terminus of the human TYMS.
  • Target Species
  • Human, Mouse, Rat
  • Bead Capacity
  • 40 mg/mL
  • Bead size
  • 25 μm
  • Format
  • Suspension
  • Concentration
  • 2 mg/mL
  • Buffer
  • PBS, pH 7.4
  • Preservative
  • 0.1% Sodium azide
  • Storage
  • Stored at 4°C, and is stable for up to 2 years. Do not centrifuge, dry or freeze the magnetic beads.

Applications

  • Application Notes
  • The beads are in suspension and will settle upon storage. Prior to use, mix the vial gently (do not vortex) to ensure delivery of proper bead volume.

Target

  • Introduction
  • Thymidylate synthase catalyzes the methylation of deoxyuridylate to deoxythymidylate using, 10-methylenetetrahydrofolate (methylene-THF) as a cofactor. This function maintains the dTMP (thymidine-5-prime monophosphate) pool critical for DNA replication and repair. The enzyme has been of interest as a target for cancer chemotherapeutic agents. It is considered to be the primary site of action for 5-fluorouracil, 5-fluoro-2-prime-deoxyuridine, and some folate analogs. Expression of this gene and that of a naturally occurring antisense transcript, mitochondrial enolase superfamily member 1 (GeneID:55556), vary inversely when cell-growth progresses from late-log to plateau phase. Polymorphisms in this gene may be associated with etiology of neoplasia, including breast cancer, and response to chemotherapy. [provided by RefSeq, Aug 2017]
  • Alternative Names
  • Thymidylate Synthetase; EC 2.1.1.45; TSase; TS; Thymidylate Synthase; HST422; TMS;
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