COR47 Antibody

Shipped with Ice Packs
In Stock

Description

Clarification of Terminology

CD47 Antibody (often mistaken for "COR47" due to potential typographical errors) is a well-established therapeutic target in oncology. CD47 is a transmembrane protein that inhibits macrophage-mediated phagocytosis by binding to SIRPα on immune cells. Anti-CD47 antibodies block this interaction, enabling immune clearance of cancer cells .

Key Anti-CD47 Antibodies in Development

Below are prominent anti-CD47 antibodies under investigation, supported by clinical and preclinical data:

Antibody NameDeveloper/StudyMechanism & TargetClinical PhaseKey Findings
Magrolimab (5F9)Gilead SciencesHumanized IgG4 anti-CD47Phase IIICombined with azacitidine shows 52% ORR in AML ; anemia/thrombocytopenia reported
IMC-002ImmuneOnciaIgG4 with minimal RBC bindingPhase I50% disease control rate in solid tumors; no anemia/thrombocytopenia
CC-90002Celgene/Bristol MyersHumanized IgG4 anti-CD47Phase I (Terminated)Lack of monotherapy efficacy in AML/MDS
IBI322Innovent BiologicsCD47/PD-L1 bispecific antibodyPhase I47.8% ORR in cHL; lymphopenia as main AE
ZF1Academic ResearchFully human anti-CD47 from phage libraryPreclinicalInduces phagocytosis in leukemia models

3.1. CD47-SIRPα Axis Blockade

Anti-CD47 antibodies disrupt the "don’t eat me" signal by preventing CD47-SIRPα interaction, enhancing macrophage phagocytosis of tumor cells . Fc engineering (e.g., GAALIE variant) optimizes binding to activating FcγRs, improving efficacy while reducing toxicity .

3.2. Combination Therapies

  • With Checkpoint Inhibitors: Synergy observed with PD-1/PD-L1 inhibitors via enhanced T-cell activation .

  • With Chemotherapy: Increased tumor cell opsonization improves phagocytosis in AML and MDS .

4.1. Toxicity Profile

  • Hematologic Toxicity: Anemia and thrombocytopenia due to CD47 expression on RBCs and platelets .

  • Mitigation Strategies: IMC-002’s engineered Fc minimizes RBC binding, reducing toxicity .

4.2. Biomarker-Driven Approaches

  • CD47+ Macrophage Density: Correlates with clinical benefit in IMC-002 trials (71.0/mm² vs. 44.3/mm² in non-responders) .

  • FcγR Polymorphisms: Influence antibody efficacy; humanized mouse models aid preclinical optimization .

Future Directions

  1. Bispecific Antibodies: IBI322 (CD47/PD-L1) shows promise in relapsed Hodgkin’s lymphoma .

  2. Localized Delivery: Intratumoral administration reduces systemic toxicity while enhancing abscopal effects .

  3. AI-Driven Biomarkers: Platforms like Lunit SCOPE IO identify responders via macrophage density analysis .

Product Specs

Buffer
Preservative: 0.03% ProClin 300; Constituents: 50% Glycerol, 0.01M Phosphate Buffered Saline (PBS), pH 7.4
Form
Liquid
Lead Time
14-16 week lead time (made-to-order)
Synonyms
COR47 antibody; RD17 antibody; At1g20440 antibody; F5M15.22Dehydrin COR47 antibody; Cold-induced COR47 protein antibody
Target Names
COR47
Uniprot No.

Q&A

FAQs for COR47 Antibody Research (Academic Focus)

Advanced Research Questions

How to resolve contradictions in COR47 localization data across studies?

  • Hypothesis-driven troubleshooting:

    • Assess antibody clonality: Polyclonal vs. monoclonal antibodies may differ in epitope recognition .

    • Evaluate stress conditions: Subcellular shifts may occur depending on stress duration (e.g., acute vs. chronic cold exposure) .

    • Use subcellular fractionation + mass spectrometry to confirm compartment-specific abundance .

What strategies optimize COR47 antibody performance in plant tissue-specific profiling?

  • Employ tissue-preferred promoters (e.g., root vascular-specific) in transgenic lines to isolate context-dependent expression .

  • Combine flow cytometry (for single-cell resolution) with RNA-seq to correlate protein and transcript levels .

How to design a study analyzing COR47’s role in nitrogen assimilation under cold stress?

  • Experimental framework:

    • Generate COR47 knockdown/overexpression lines using CRISPR or dexamethasone-inducible systems .

    • Quantify nitrate reductase activity and glutamine synthetase levels under mild cold (4°C) .

    • Pair with transient transformation assays to test COR47 interaction with nitrogen-responsive TFs (e.g., NLP7) .

Data Contradiction Analysis

Conflicting reports on COR47’s role in drought vs. cold adaptation: How to reconcile?

  • Systematic review approach:

    • Stratify studies by stress severity: COR47 may have dual roles depending on stress intensity .

    • Analyze antibody batches: Variability in affinity purification can cause functional discrepancies .

    • Use bimolecular fluorescence complementation (BiFC) to test COR47 interaction partners under differing stress conditions .

Can COR47 antibody cross-react with homologs in non-model species?

  • Epitope mapping:

    • Synthesize COR47-derived peptides spanning variable regions (e.g., residues 120-150).

    • Test reactivity via SPOT array against homologs from phylogenetically diverse species .

    • Cite sequence alignment tools (e.g., Clustal Omega) to identify conserved domains .

How to assess post-translational modifications (PTMs) of COR47 using antibody-based methods?

  • PTM-specific protocols:

    • Phosphorylation: Treat lysates with λ-phosphatase + Western blot .

    • Ubiquitination: Co-immunoprecipitate with ubiquitin antibodies under proteasome inhibition .

Methodological Innovations

What transient expression systems improve COR47 antibody validation throughput?

  • Adopt TARGET (Transient Assay Reporting Genome-wide Effects) :

    • Fuse COR47 to glucocorticoid receptor (GR) for dexamethasone-inducible nuclear translocation.

    • Use RNase H-dependent PCR to quantify direct transcriptional targets within 48h .

How to integrate COR47 antibody data with multi-omics datasets?

  • Workflow:

    • Align antibody-derived protein levels with RNA-seq (transcriptome) and LC-MS (metabolome).

    • Apply weighted gene co-expression network analysis (WGCNA) to identify stress-responsive modules .

    • Validate candidates via virus-induced gene silencing (VIGS) + phenotyping .

Key Citations

  • Tissue-specific promoters for context-dependent studies .

  • Cycloheximide controls in transient assays .

  • Antibody reformatting/humanization for reduced cross-reactivity .

  • TARGET system for rapid TF-target identification .

Quick Inquiry

Personal Email Detected
Please use an institutional or corporate email address for inquiries. Personal email accounts ( such as Gmail, Yahoo, and Outlook) are not accepted. *
© Copyright 2025 TheBiotek. All Rights Reserved.