Anti-Human HMG1 Recombinant Antibody scFv Fragment (TAB-100CT-S(P))

CAT#: TAB-100CT-S(P)

Recombinant monoclonal antibody to HMG1. This antibody intended for the prophylaxis and treatment of HMGB1-related diseases .

Gene Expression
Figure 1 IF staining of human cell line RH-30 Figure 2 IF staining of human cell line A-431 Figure 3 IHC staining of human bone marrow Figure 4 IHC staining of human esophagus Figure 5 IF staining of human cell line U-2 OS Figure 6 IF staining of human cell line U-251 MG Figure 7 Cerebral cortex Figure 8 Colon Figure 9 Liver Figure 10 Kidney Figure 11 Lymph node Figure 12 RNA cell line category: Low cell line specificity

Specifications

  • Immunogen
  • 17-mer peptide P1 (KGKPDAAKKGVVKAEKS)
  • Host Species
  • Mouse
  • Derivation
  • Hybridoma cell line
  • Specificity
  • Human
  • Species Reactivity
  • Human
  • Applications
  • WB, IF, FC, FuncS, Transmigration assay
  • Related Disease
  • HMGB1-related diseases

Applications

  • Application Notes
  • Anti-HMGB-1 Ab (DPH1.1 Ab) characterization and specificity testing by Western blot
    Western blots of the recombinant BoxA domain of HMGB1 (negative control) incubated with either the anti-HMGB-1 mAb DPH1.1 or a control anti-BoxA mAb control were performed. Briefly, 500 ng or 100 ng of recombinant HMGB1 and the (negative control) recombinant BoxA domain of HMGB1 were separated by gel electrophoresis and transferred onto membranes.
    Immunofluorescence
    DPH1.1 mAb, anti-BoxA mAb and goat anti- mouse lgG1 Ab were applied at 1μg/ml dilution. Immunofluorescence was performed on mouse embryonic fibroblasts (MEFs) derived from either wild type mice or HmgbV¹ mice. DPH1.1 mAb and AlexaFluor 633-labelled goat anti-mouse lgG1 Ab were applied at a 50 μg/ml dilution.
    Transmigration assay
    Recombinant HMGB1 was added to the lower chamber at the concentration of 30 ng/ml. Increasing concentrations of DPH1. 1 mAb (or of an irrelevant isotype-matched mAb) were added to fifty thousand 3T3 cells. Cell migration was assessed by a modified Boyden chamber assay. Boyden chambers were incubated at 37 °C in 5% CO₂ for 3 hrs. Cells remaining on the upper section of the filters were removed mechanically. Cells that migrated to the lower section of the filters were fixed with ethanol, stained with Giemsa, and counted in 10 random fields/filter.
    In vivo experiments
    Inflammatory cell recruitment Recruitment of inflammatory cells can be amplified by removal of Kupffer cells (KCs) from the liver, which can be obtained by treatment of the mice with clodronate (Clo-L). In order to amplify the effect of HMGB1, Kupffer cells (KCs) of HBV transgenic mice were removed, and injected with CD8 T cells from mice immunized against HBV (this causes acute hepatitis in the mice).

Target

  • Alternative Names
  • HMGB1; high mobility group box 1; HMG1; HMG3; SBP-1; high mobility group protein B1; HMG-1; Amphoterin; high-mobility group box 1; high mobility group protein 1; Sulfoglucuronyl carbohydrate binding protein; high-mobility group (nonhistone chromosomal) protein 1; anti-HMGB1
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Product Notes

This is a product of Creative Biolabs' Hi-Affi™ recombinant antibody portfolio, which has several benefits including:

• Increased sensitivity
• Confirmed specificity
• High repeatability
• Excellent batch-to-batch consistency
• Sustainable supply
• Animal-free production

See more details about Hi-Affi™ recombinant antibody benefits.

Datasheet

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COA

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Protocol & Troubleshooting

We have outlined the assay protocols, covering reagents, solutions, procedures, and troubleshooting tips for common issues in order to better assist clients in conducting experiments with our products. View the full list of Protocol & Troubleshooting.

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