Human Anti-CTLA4 Recombinant Antibody (HPAB-M0042-YC)

CAT#: HPAB-M0042-YC

This product is a recombinant human antibody that recognizes Cytotoxic T lymphocyte antigen-4. The antibody can be effectively combined CTLA4 and block the interaction between CTLA4 and B7 protein. The antibody was expressed in mammalian cells with chemically defined culture media and was purified by affinity chromatography.

Gene Expression
Figure 1 RNA cell line category: Cell line enhanced (Karpas-707, SK-MEL-30, U-266/70, U-266/84)

Specifications

  • Immunogen
  • CTLA4-mFc antigen
  • Host Species
  • Human
  • Derivation
  • Humanized
  • Type
  • Humanized IgG
  • Specificity
  • Human CTLA4
  • Species Reactivity
  • Human
  • Applications
  • ELISA, FC, FuncS

Product Property

  • Purity
  • >95% as determined by SDS-PAGE
  • Concentration
  • Please refer to the vial label for the specific concentration.
  • Buffer
  • PBS
  • Preservative
  • No preservatives
  • Storage
  • Centrifuge briefly prior to opening vial. Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

  • Alternative Names
  • Cytotoxic T-Lymphocyte Associated Protein 4; Insulin-Dependent Diabetes Mellitus 12; Celiac Disease 3; CTLA-4; CD152; Ligand And Transmembrane Spliced Cytotoxic T Lymphocyte Associated Antigen 4; Cytotoxic T Lymphocyte Associated Antigen 4 Short Spliced Form; Cytotoxic T-Lymphocyte-Associated Serine Esterase-4; Cytotoxic T-Lymphocyte-Associated Antigen 4; Cytotoxic T-Lymphocyte Protein 4;
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Citations

  1. Wiese, Teresa. Pharmacological targeting of acid sphingomyelinase increases CD4\(^+\) Foxp3\(^+\) regulatory T cell subsets in patients with major depression. Diss. Universität Würzburg, 2022. https://doi.org/10.25972/OPUS-23347
    This research investigates the effects of acid sphingomyelinase (ASM) inhibition on regulatory T cell (Treg) populations in humans. The study demonstrates that pharmacological inhibition of ASM, particularly through antidepressants with strong ASM-inhibitory capacity, leads to increased frequencies of effector regulatory T cells (efTregs) among CD4+ T cells both in vitro and in patients treated for major depression. The researchers found that ASM inhibition enhances CD28 co-stimulation in Tregs, promoting their survival without affecting their suppressive function. Additionally, the study identified an early increase in efTreg frequencies as a potential biomarker for positive clinical response to antidepressant treatment, independent of the drug's ASM-inhibitory capacity. These findings suggest that ASM inhibition could be therapeutically beneficial for autoimmune diseases characterized by reduced Treg frequencies.
    Creative Biolabs provided the CTLA-4 inhibiting monoclonal antibody tremelimumab and the PD-1 inhibiting monoclonal antibody pembrolizumab, which were crucial for understanding the mechanistic relationship between immune checkpoint inhibition and ASM activity. These antibodies allowed the researchers to demonstrate that both ASM inhibition and CTLA-4 blockade increase efTreg frequencies through a common CD28-dependent pathway, providing key insights into how ASM modulates T cell homeostasis and identifying potential therapeutic targets for inflammatory and autoimmune conditions.

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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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