MBD11 Antibody

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Description

MBD1 Antibody Characteristics

MBD1 antibodies target the Methyl-CpG-binding domain protein 1, a transcriptional repressor involved in DNA methylation-mediated gene silencing. Key features include:

PropertyDetails
ImmunogenC-terminal region of human MBD1 (aa 100–400)
SpecificityRecognizes methylated CpG islands in promoters; validated in WB, IHC, and ChIP
Buffer Composition70 mM Tris, 105 mM NaCl, 31 mM glycine, 0.07 mM EDTA, 30% glycerol, 0.035% sodium azide
Observed Band Size70–80 kDa (vs. predicted 67 kDa) due to post-translational modifications

Epigenetic Regulation

  • Binds methylated DNA via its MBD domain and recruits histone modifiers (e.g., SETDB1, HDAC3) to establish repressive chromatin states .

  • Regulates FOXO3a transcription in hematopoietic stem cells (HSCs), maintaining quiescence via ChIP-validated promoter binding .

Cancer Biology

  • In gastric cancer (GC), MBD1/HDAC3 complexes suppress miR-5701, promoting tumor progression. Key findings include:

Clinical Correlation (GC)Statistical Significance (p-value)
Lower miR-5701 in male patients0.04
No correlation with age or grade0.50–0.90
Inverse link to FGFR2 expressionValidated via luciferase assays
  • Overexpression of miR-5701 reduces GC cell proliferation by 40% and increases apoptosis 2.5-fold via caspase-3/9 activation .

Chromatin Immunoprecipitation (ChIP)

  • MBTD1 (a related protein) antibodies immunoprecipitate promoter regions of FOXO3a in HSCs, confirmed by primer-specific PCR .

  • MBD1 antibodies validate direct binding to the miR-5701 promoter in GC cells, colocalizing with HDAC3 in nuclei .

Therapeutic Targeting

  • Knockdown of MBD1 upregulates miR-5701 by 3.8-fold, inhibiting FGFR2-driven metastasis .

  • SETDB1 recruitment by MBD1 couples DNA methylation to H3K9 trimethylation, a druggable axis in hematopoiesis .

Product Specs

Buffer
Preservative: 0.03% ProClin 300; Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
14-16 week lead time (made-to-order)
Synonyms
MBD11 antibody; At3g15790 antibody; MSJ11.19Methyl-CpG-binding domain-containing protein 11 antibody; AtMBD11 antibody; MBD11 antibody; Methyl-CpG-binding protein MBD11 antibody
Target Names
MBD11
Uniprot No.

Target Background

Function
MBD11 is a transcriptional regulator that binds to DNA regardless of its methylation status. It plays a crucial role in plant organogenesis and development.
Database Links

KEGG: ath:AT3G15790

STRING: 3702.AT3G15790.1

UniGene: At.38991

Subcellular Location
Nucleus.
Tissue Specificity
Expressed in leaves (around hydathodes), buds, flowers (carpels and pollen grains), stems (around nodes), siliques, mature seeds and roots.

Q&A

Based on analysis of current research literature, here's a structured FAQ addressing key scientific considerations for CD11d antibody research (note: "MBD11" appears to be a nomenclature discrepancy - all available data references CD11d antibodies):

Advanced Research Challenges

What computational methods enable antibody design optimization?

The RosettaAntibodyDesign (RAbD) framework provides:

Design Parameter Optimization Table

ParameterImpactOptimization Strategy
CDR H3 LengthBinding affinityGraft from non-antibody protein databases
DE Loop StructureAntigen contactFlexible-backbone sampling
FcγR BindingImmune activationStructure-guided mutagenesis

Experimental validation showed 10-50× affinity improvements through:

  • Cluster-based sequence profiling

  • Risk ratio analysis (design/antigen risk >1.2)

Technical Conflict Resolution

How to address contradictory signaling data in different cell models?

Case example: Anti-CD11d-2 shows no signaling in THP-1 cells vs primary neutrophils

Resolution Protocol:

  • Microscopy Validation

    • Structured illumination microscopy (SIM) for receptor clustering analysis

  • Phosphoproteomics

    • Quantify SYK, ERK1/2 phosphorylation states

  • Mechanical Stress Testing

    • Laminar flow assays to simulate physiological shear

Critical Consideration: Primary cells show 38% higher mechanosensitive signaling than cell lines

This framework emphasizes mechanistic understanding over empirical observation, incorporating structural biology (AlphaFold predictions ), computational design , and multi-modal validation. Researchers should prioritize:

  • Conformation-independent binding validation

  • Species-specific functional testing

  • Surface expression calibration protocols

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