At2g18620 Antibody

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Description

Definition and Basic Characteristics

The At2g18620 Antibody (Product Code: CSB-PA124356XA01DOA) is a polyclonal antibody raised against the protein encoded by the At2g18620 locus in Arabidopsis thaliana. This gene is annotated in the UniProt database under accession Q9ZU77, though its precise molecular function remains under investigation. The antibody is produced in standardized volumes (2 mL or 0.1 mL) and is validated for applications such as Western blotting, immunohistochemistry, and ELISA .

Research Applications

The At2g18620 Antibody is primarily utilized to:

  • Map Protein Expression: Identify spatial and temporal expression patterns of the At2g18620 protein in Arabidopsis tissues .

  • Study Subcellular Localization: Determine cellular compartments where the protein accumulates (e.g., nucleus, cytoplasm) via immunofluorescence .

  • Investigate Protein Interactions: Support pull-down assays to identify binding partners or post-translational modifications .

Comparative Data on Related Antibodies

The At2g18620 Antibody belongs to a broader catalog of Arabidopsis-targeting reagents. Below is a subset of related antibodies for context :

Product NameTarget GeneUniProt IDApplications
GONST2 AntibodyGONST2Q84L09WB, IHC
GOLS10 AntibodyGOLS10F4KED2ELISA, IF
At2g18620 AntibodyAt2g18620Q9ZU77WB, IHC, ELISA

Challenges and Future Directions

  • Functional Annotation: The At2g18620 protein lacks detailed functional characterization, necessitating studies using knockout mutants alongside antibody-based assays .

  • Technical Optimization: Advances in antibody engineering, such as affinity maturation or epitope tagging, could improve detection limits .

Validation and Quality Control

The antibody’s specificity is typically confirmed using:

  • Knockout Controls: Comparison of signal in wild-type vs. At2g18620 mutant plants.

  • Peptide Blocking: Pre-incubation with the immunizing peptide to abolish signal .

Product Specs

Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M Phosphate Buffered Saline (PBS), pH 7.4
Form
Liquid
Lead Time
Made-to-order (14-16 weeks)
Synonyms
At2g18620 antibody; F24H14.3Geranylgeranyl pyrophosphate synthase 7 antibody; chloroplastic antibody; GGPP synthase 7 antibody; GGPS7 antibody; EC 2.5.1.-; antibody; 2E,6E)-farnesyl diphosphate synthase 7 antibody; Dimethylallyltranstransferase 7 antibody; EC 2.5.1.1 antibody; Farnesyl diphosphate synthase 7 antibody; Farnesyltranstransferase 7 antibody; EC 2.5.1.29 antibody; Geranyltranstransferase 7 antibody; EC 2.5.1.10 antibody
Target Names
At2g18620
Uniprot No.

Target Background

Function
This antibody targets At2g18620, an enzyme that catalyzes the trans-addition of three molecules of isopentenyl pyrophosphate (IPP) onto dimethylallyl pyrophosphate (DMAPP) to form geranylgeranyl pyrophosphate.
Database Links

KEGG: ath:AT2G18620

STRING: 3702.AT2G18620.1

UniGene: At.52813

Protein Families
FPP/GGPP synthase family
Subcellular Location
Plastid, chloroplast.

Q&A

Here’s a structured collection of FAQs tailored for academic researchers working with the At2g18620 antibody, integrating methodological guidance and data-driven insights from peer-reviewed studies:

Advanced Research Questions

  • What structural features of At2g18620 influence antibody-antigen binding?

    • Use deep-learning models (trained on antibody-antigen interfaces, as in ) to predict epitope regions.

    • Perform alanine scanning mutagenesis on At2g18620 to identify critical binding residues.

  • How do I design a study to assess At2g18620’s role in carotenoid biosynthesis?

    • Experimental workflow:

      1. Generate transgenic Arabidopsis lines overexpressing At2g18620.

      2. Quantify carotenoids via HPLC (methods in ).

      3. Correlate expression levels (via qPCR/Western blot) with metabolite profiles.

    • Key controls: Use mutants defective in downstream enzymes (e.g., lycopene cyclase ).

  • What computational tools can enhance At2g18620 antibody validation?

    • Implement graph convolutional networks (as in ) to predict antibody-antigen interaction strength.

    • Use molecular dynamics simulations to model binding stability under varying pH/temperature conditions.

Table 1: Comparison of Antibody Validation Methods

MethodSensitivitySpecificityThroughputKey Application
ImmunoblottingModerateHighLowInitial specificity screening
Surface Plasmon Resonance (SPR)HighVery HighMediumAffinity quantification
ELISAHighModerateHighCross-reactivity profiling

Table 2: Common Cross-Reactive Species for At2g18620 Antibody

SpeciesHomology (%)Likelihood of Cross-Reactivity
Brassica oleracea89%High
Arabidopsis lyrata95%Very High
Glycine max72%Low

Methodological Best Practices

  • For epitope mapping: Combine hydrogen-deuterium exchange mass spectrometry (HDX-MS) with SPR-based binding assays (as in ) to resolve conformational epitopes.

  • To address batch variability: Pre-absorb antibodies against lysates from knockout models to remove nonspecific binders.

  • In functional studies: Use dual-labeling immunofluorescence with organelle-specific markers to localize At2g18620 in planta.

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