AbPlus™ Anti-TTR Magnetic Beads (AD7F6)

CAT#: VS-0424-XY265

The AbPlus Anti-TTR Magnetic Beads (AD7F6) is an innovative affinity resin which is bound with anti-TTR specific antibody (AD7F6). The beads were designed for small-scale affinity purification and immunoprecipitation (IP) of TTR protein under native and denaturing conditions.

Gene Expression
Figure 1 IF staining of human cell line CACO-2 Figure 2 IHC staining of human hippocampus Figure 3 IHC staining of human liver Figure 4 IHC staining of human pancreas Figure 5 IHC staining of human kidney Figure 6 Liver Figure 7 Pancreas Figure 8 Kidney Figure 9 RNA cell line category: Cell line enhanced (CACO-2, EFO-21, Hep G2, U-2 OS)

Specifications

  • Applications
  • Immunoprecipitation, Protein Purification
  • Matrix
  • Magrose bead (> 50 μmol/mL gel)
  • Bead Ligand
  • Anti-TTR specific antibody (AD7F6)
  • Target
  • TTR
  • Immunogen
  • Recombinant mutant TTR (Y78F)
  • Target Species
  • Human
  • Antibody Clone
  • AD7F6
  • Bead Capacity
  • 20-30 mg/mL binding antibody
  • Bead size
  • 10-37 μm
  • Stability
  • pH 2-14
  • Format
  • 20% Suspension
  • Buffer
  • PBS, pH 7.4, with 1% BSA
  • Preservative
  • 0.03% Proclin 300
  • 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
  • This gene encodes one of the three prealbumins, which include alpha-1-antitrypsin, transthyretin and orosomucoid. The encoded protein, transthyretin, is a homo-tetrameric carrier protein, which transports thyroid hormones in the plasma and cerebrospinal fluid. It is also involved in the transport of retinol (vitamin A) in the plasma by associating with retinol-binding protein. The protein may also be involved in other intracellular processes including proteolysis, nerve regeneration, autophagy and glucose homeostasis. Mutations in this gene are associated with amyloid deposition, predominantly affecting peripheral nerves or the heart, while a small percentage of the gene mutations are non-amyloidogenic. The mutations are implicated in the etiology of several diseases, including amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis and carpal tunnel syndrome.
  • Alternative Names
  • Transthyretin; Prealbumin, Amyloidosis Type I; PALB; ATTR; TBPA; Epididymis Luminal Protein 111; Thyroxine-Binding Prealbumin
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