Anti-Human HMG1 Recombinant Antibody (DPH1 .1 mAb) (CAT#: TAB-100CT)

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


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Figure 1 shows representative western blots of recombinant BoxA fragment of HMGB1 with the anti-HMGB1 mAb DPH1.1.

Figure 1 shows representative western blots of recombinant BoxA fragment of HMGB1 with the anti-HMGB1 mAb DPH1.1.

500 ng (lane 1) or 100 ng (lane 2) of the recombinant BoxA fragment of HMGB1 (negative control) and 500 ng (lane 3) or 100 ng (lane 4) of recombinant HMGB1 incubated with either the anti-HMGB1 mAb DPH1.1 (top panel) or a control anti-Box-A subunit Ab control (bottom panel).

Figure 2 Immunofluorescence of anti-HMGB1 mAb DPH1.1

Figure 2 Immunofluorescence of anti-HMGB1 mAb DPH1.1

shows representative micrographs of mouse embryonic fibroblasts (MEFs) derived from either wild type (wt) mice or Hmgbl-/- mice that were stained by immunofluorescence with the anti-HMGB1 mAb DPH1.1.

Figure 3 shows migration of 3T3 cells towards HMGB1 in the presence of the indicated concentrations of the anti-HMGB1 mAb, examined using a modified Boyden chamber assay.

Figure 3 shows migration of 3T3 cells towards HMGB1 in the presence of the indicated concentrations of the anti-HMGB1 mAb, examined using a modified Boyden chamber assay.

Figure 4 shows the results of the in vivo experiments of inflammatory cell recruitment.

Figure 4 shows the results of the in vivo experiments of inflammatory cell recruitment.

Figure 5 are representative graphs of the results of the in vivo experiments.

Figure 5 are representative graphs of the results of the in vivo experiments.

In particular, sALT levels in the blood (Figure A) and absolute number of Gr-1ʰ ⁱᵍʰ CD11 b⁺ neutrophils (PMNs) recovered from the livers (Figure B) of 6 HBV transgenic mice that received NaCI (white squares), Clo-L and irrelevant (Irr) lgG1 mAb (black triangles) or Clo-L and the anti-HMGB1 mAb DPH1.1 (black circles) along with the intravenous injection of 10⁷ HBV-specific CTLs.


Specifications

  • Immunogen
  • 17-mer peptide P1 (KGKPDAAKKGVVKAEKS)
  • Host Species
  • Mouse
  • Derivation
  • Hybridoma cell line
  • Specificity
  • Human
  • Species Reactivity
  • Human
  • Clone
  • DPH1 .1 mAb
  • 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

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.

Downloads

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Humanized Antibody

Human Antibody

CAT Product Name Application Type
TAB-101CT Anti-Human HMG1 Recombinant Antibody ELISA, BL Human antibody
TAB-101CT-S(P) Anti-Human HMG1 Recombinant Antibody scFv Fragment ELISA, BL Human antibody
TAB-101CT-F(E) Anti-Human HMG1 Recombinant Antibody Fab Fragment ELISA, BL Human antibody

Rabbit Monoclonal Antibody

CAT Product Name Application Type
MOR-1633 Rabbit Anti-HMGB1 Recombinant Antibody (clone DS1633AB) WB, IHC-P, FC Rabbit IgG
MOR-0049-FY Rabbit Anti-HMGB1 Recombinant Antibody (clone AFY0020) ICC, IHC-P, WB Rabbit IgG

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For Research Use Only. Not For Clinical Use.

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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