AbPlus™ Anti-HSPD1 Magnetic Beads (VS-0724-YC1197)

CAT#: VS-0724-YC1197

The AbPlus Anti-HSPD1 Magnetic Beads (VS-0724-YC1197) is an innovative affinity resin which is bound with anti-HSPD1 specific antibody. The beads were designed for small-scale affinity purification and immunoprecipitation (IP) of HSPD1 protein under native and denaturing conditions.

Gene Expression
Figure 1 IF staining of human cell line U-251 MG Figure 2 IF staining of human cell line A-431 Figure 3 IHC staining of human kidney Figure 4 IHC staining of human rectum Figure 5 IHC staining of human colon Figure 6 IF staining of human cell line U-2 OS Figure 7 Cerebral cortex Figure 8 Colon Figure 9 Liver Figure 10 Pancreas Figure 11 Kidney Figure 12 Testis Figure 13 RNA cell line category: Low cell line specificity

Specifications

  • Applications
  • Immunoprecipitation, Protein Purification
  • Matrix
  • Magnetic bead
  • Bead Ligand
  • Anti-HSPD1 specific antibody
  • Target
  • HSPD1
  • Immunogen
  • Synthetic peptide corresponding to the C-terminus of the human HSPD1/HSP60.
  • Target Species
  • Human
  • 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
  • This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. [provided by RefSeq, Jun 2010]
  • Alternative Names
  • Heat Shock Protein Family D (Hsp60) Member 1; Heat Shock 60kDa Protein 1 (Chaperonin); Mitochondrial Matrix Protein P1; P60 Lymphocyte Protein; 0 KDa Chaperonin; Chaperonin 60; HuCHA60; HSP-60; HSP60; CPN60; Spastic Paraplegia 13 (Autosomal Dominant);
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For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.

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