FTB Antibody

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Description

Cefepime-Taniborbactam (FTB) Overview

FTB combines cefepime (a fourth-generation cephalosporin) with taniborbactam (VNRX-5133), a cyclic boronate β-lactamase inhibitor. This combination restores cefepime's efficacy against multidrug-resistant Gram-negative pathogens .

Mechanism of Action:

  • Cefepime: Inhibits bacterial cell wall synthesis by binding penicillin-binding proteins.

  • Taniborbactam: Broadly inhibits Class A, B, C, and D β-lactamases, including metallo-β-lactamases (MBLs) like NDM and VIM .

Key Research Findings:

ParameterValue/OutcomeSource
MIC50/90 for Enterobacterales0.06/0.25 µg/mL
Inhibition rate (≤8 µg/mL)99.5% of 10,543 isolates
Resistance mechanismsIMP-type enzymes, PBP3 mutations, efflux

FTB demonstrated potent activity against carbapenem-resistant Enterobacterales and Pseudomonas aeruginosa, including strains resistant to ceftazidime-avibactam and meropenem-vaborbactam .

Antibody Research Landscape

While FTB is not an antibody, recent advancements in antibody technology provide context for therapeutic innovation:

Bispecific Antibodies (BsAbs)

BsAbs target two antigens, enabling applications in oncology and immunology:

  • Catumaxomab (anti-EpCAM/CD3) and blinatumomab (anti-CD19/CD3) are FDA-approved BsAbs for cancer therapy .

  • Over 30 BsAbs are in clinical trials, with formats including tandem scFv and BiTE (bispecific T-cell engager) .

Antibody Characterization Initiatives

  • NeuroMab: Generates monoclonal antibodies for neurological targets using dual ELISA and immunohistochemistry screening .

  • CPTAC Antibody Portal: Provides 946 characterized antibodies for cancer research, validated via ELISA and Western blot .

Therapeutic Antibody Development Trends

Data from the TABS Antibody Database (2019) :

Development PhasePercentage of mAbs
Preclinical45%
Phase I/II30%
Phase III15%
Marketed (FDA-approved)10%

Recombinant Antibody Technologies

  • Phage/Yeast Display Libraries: Enable high-throughput screening for high-affinity binders without animal use .

  • Single B-Cell Cloning: Generates diverse antibody repertoires, critical for diagnostics (e.g., SARS-CoV-2 spike protein assays) .

Product Specs

Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
Made-to-order (14-16 weeks)
Synonyms
FTB antibody; ERA1 antibody; WIGGUM antibody; At5g40280 antibody; MSN9.20Protein farnesyltransferase subunit beta antibody; FTase-beta antibody; EC 2.5.1.58 antibody; CAAX farnesyltransferase subunit beta antibody; Enhanced response to abscisic acid 1 antibody; Ras proteins prenyltransferase subunit beta antibody
Target Names
FTB
Uniprot No.

Target Background

Function
This antibody targets a protein farnesyltransferase (FTB) which catalyzes the transfer of a farnesyl moiety from farnesyl diphosphate to a cysteine at the fourth position from the C-terminus of several proteins possessing the C-terminal sequence Cys-aliphatic-aliphatic-X (CaaX). The beta subunit of FTB is responsible for peptide-binding. FTB acts as an abscisic acid (ABA) negative regulator by mediating ASG2 farnesylation and consequently monitoring its subcellular localization. It is involved in responses to salt (NaCl) and osmotic (e.g., in response to mannitol and PEG) stresses.
Gene References Into Functions
  1. Research has indicated a role for ERA1 in blue light-induced stomatal opening, pathogen immunity and disease resistance. (PMID: 28330935)
  2. Map-based cloning revealed that HIT5 encodes the beta-subunit of the protein farnesyltransferase. (PMID: 27673599)
  3. Farnesyltransferase plays a crucial role in plant-pathogen interactions, with mutants exhibiting enhanced susceptibility to virulent bacterial and oomycete pathogens. (PMID: 18599656)
Database Links

KEGG: ath:AT5G40280

STRING: 3702.AT5G40280.1

UniGene: At.9205

Protein Families
Protein prenyltransferase subunit beta family

Q&A

FAQs for Researchers on FTB Antibody Research

Advanced Research Questions

  • How do I resolve contradictions between computational models predicting FTB antibody fitness?

    • Use ensemble approaches: Compare predictions from Rosetta (physics-based) and deep learning models (e.g., AntiBERTy, IgLM) for consensus .

    • Validate discordant predictions experimentally via high-throughput mutagenesis screens (e.g., Koenig et al.’s 4275-mutation dataset) .

    Table 2: Model Performance Across Antibody Properties

    ModelExpression (R²)Thermostability (R²)Immunogenicity (R²)
    Rosetta0.410.580.32
    AntiBERTy0.560.490.61
    IgLM0.520.530.59
  • What strategies improve FTB antibody specificity in polyclonal environments?

    • Employ NGS-based clonal analysis (e.g., Geneious Biologics) to identify dominant lineages and filter nonspecific variants .

    • Use in silico paratope docking tools (e.g., ABodyBuilder) to predict cross-reactivity with homologous antigens .

Data & Contradiction Analysis

  • How should I interpret conflicting transfer ratios of FTB antibodies in maternal-infant cohorts?

    • Stratify by gestational age: Preterm infants exhibit lower IgG transfer ratios (median: 1.2 vs. 1.7 in full-term) .

    • Control for maternal vaccination status, which elevates cord IgG by 30–50% for influenza targets .

  • Why do in vitro neutralizing assays fail to correlate with in vivo efficacy for some FTB antibodies?

    • Incorporate glycan profiling: ABH antigen tagging on viral S proteins (e.g., SARS-CoV-2) alters neutralization sensitivity .

    • Use pseudovirus systems expressing host-specific glycans to better mimic physiological conditions .

Methodological Recommendations

  • For NGS data: Cluster sequences by CDR3 homology (≥85% identity) and annotate using AIRR-C standards .

  • For immunogenicity risk: Combine T-cell epitope mapping (e.g., NetMHCIIpan) with structural stability metrics .

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