Recombinant Drosophila melanogaster Actin-related protein 3 (Arp66B)

Shipped with Ice Packs
In Stock

Product Specs

Form
Lyophilized powder. We will preferentially ship the format we have in stock. If you have special format requirements, please note them when ordering, and we will fulfill your request.
Lead Time
Delivery times may vary depending on the purchasing method and location. Please consult your local distributors for specific delivery times. All proteins are shipped with normal blue ice packs by default. For dry ice shipping, please contact us in advance, and additional fees will apply.
Notes
Avoid repeated freezing and thawing. Working aliquots can be stored at 4°C for up to one week.
Reconstitution
Briefly centrifuge the vial before opening to collect the contents at the bottom. Reconstitute the protein in sterile deionized water to a concentration of 0.1-1.0 mg/mL. Adding 5-50% glycerol (final concentration) and aliquoting for long-term storage at -20°C/-80°C is recommended. Our default final glycerol concentration is 50% for your reference.
Shelf Life
Shelf life depends on several factors, including storage conditions, buffer components, storage temperature, and protein stability. Generally, the liquid form has a shelf life of 6 months at -20°C/-80°C, while the lyophilized form has a shelf life of 12 months at -20°C/-80°C.
Storage Condition
Store at -20°C/-80°C upon receipt. Aliquot for multiple uses. Avoid repeated freeze-thaw cycles.
Tag Info
The tag type will be determined during the manufacturing process. If you have a specific tag type requirement, please inform us, and we will prioritize developing the specified tag.
Synonyms
Arp3; Actr66B; Arp66B; CG7558Actin-related protein 3; Actin-2; Actin-like protein 3; Actin-like protein 66B
Buffer Before Lyophilization
Tris/PBS-based buffer, 6% Trehalose.
Datasheet
Please contact us to get it.
Expression Region
1-418
Protein Length
full length protein
Purity
>85% (SDS-PAGE)
Species
Drosophila melanogaster (Fruit fly)
Target Names
Arp3
Target Protein Sequence
MAGRLPACVI DVGTGYSKLG FAGNKEPQFI IPSAIAIKES ARVGDTNTRR ITKGIEDLDF FIGDEAFDAT GYSIKYPVRH GLVEDWDLME RFLEQCVFKY LRAEPEDHYF LLTEPPLNTP ENREYTAEIM FETFNVPGLY IAVQAVLALA ASWASRSAEE RTLTGIVVDS GDGVTHVIPV AEGYVIGSCI KHIPIAGRNI TSFIQSLLRE REVGIPPEQS LETAKAIKEK HCYICPDIAK EFAKYDTEPG KWIRNFSGVN TVTKAPFNVD VGYERFLGPE IFFHPEFSNP DFTIPLSEIV DNVIQNCPID VRRPLYNNIV LSGGSTMFKD FGRRLQRDIK RSVDTRLRIS ENLSEGRIKP KPIDVQVITH HMQRYAVWFG GSMLASTPEF YQVCHTKAAY EEYGPSICRH NPVFGTMT
Uniprot No.

Target Background

Function
Functions as the ATP-binding component of the Arp2/3 complex, which regulates actin polymerization. Along with an activating nucleation-promoting factor (NPF), it mediates the formation of branched actin networks. It appears to interact with the pointed end of the daughter actin filament. It is essential during embryogenesis for the anterior migration of tail hemocytes along the ventral midline.
Gene References Into Functions
Data suggests that the Wsp-Arp2/3 machinery in cyst cells influences proper microfilament organization and enables cyst attachment to the base of the testis. (PMID: 21652648)
Database Links

KEGG: dme:Dmel_CG7558

STRING: 7227.FBpp0076460

UniGene: Dm.881

Protein Families
Actin family, ARP3 subfamily
Subcellular Location
Cytoplasm, cytoskeleton.

Q&A

Data Analysis for Contradictory Results

What strategies can researchers use to analyze and reconcile contradictory data when studying actin-related proteins?

  • Approach: Use statistical methods to assess the significance of observed effects. Consider multiple experimental replicates and controls.

  • Methods: Employ meta-analysis if combining data from different studies. Investigate potential sources of variability, such as genetic background or environmental conditions.

  • Considerations: Evaluate the consistency of results across different experimental conditions and consider the role of confounding variables.

Advanced Research Questions: Evolutionary Conservation

How does the evolutionary conservation of actin-related proteins like Arp66B inform our understanding of their functional roles?

  • Approach: Compare protein sequences across different species to identify conserved domains or motifs.

  • Methods: Use bioinformatics tools for sequence alignment and phylogenetic analysis.

  • Considerations: Investigate whether conserved regions are associated with specific functions or interactions.

Methodological Considerations for Protein Localization Studies

What methods are most effective for studying the localization of actin-related proteins in Drosophila tissues?

  • Approach: Use fluorescence microscopy with specific antibodies or tagged proteins (e.g., GFP) to visualize localization.

  • Methods: Optimize fixation and staining protocols to preserve protein localization patterns.

  • Considerations: Validate antibody specificity and ensure that tagging does not alter protein function.

Basic Questions: Role of Actin-Related Proteins in Cellular Processes

What are the primary roles of actin-related proteins in cellular processes, and how do they differ from canonical actin?

  • Approach: Review literature on known functions of actin-related proteins in processes like cytoskeleton organization, chromatin remodeling, and cell division.

  • Methods: Investigate specific examples of actin-related proteins involved in these processes.

  • Considerations: Note that actin-related proteins often function in complexes with other proteins and may have specialized roles distinct from actin.

Advanced Research Questions: Genetic Variation and Recombination

How does genetic variation, such as that affecting recombination rates, impact the study of actin-related proteins in Drosophila?

  • Approach: Use genetic mapping techniques to identify genetic variants associated with phenotypic variation in actin-related protein function.

  • Methods: Employ genome-wide association studies (GWAS) or quantitative trait locus (QTL) mapping.

  • Considerations: Account for potential interactions between genetic background and environmental factors influencing protein function.

Methodological Answers: Expression and Purification of Recombinant Proteins

What methods are used to express and purify recombinant actin-related proteins like Arp66B for biochemical studies?

  • Approach: Use bacterial or insect cell expression systems to produce recombinant proteins.

  • Methods: Employ affinity chromatography (e.g., His-tag) for purification. Validate protein integrity using techniques like SDS-PAGE and mass spectrometry.

  • Considerations: Optimize expression conditions to maximize yield and ensure proper protein folding.

Data Interpretation: Functional Assays for Actin-Related Proteins

How do researchers interpret data from functional assays designed to study the roles of actin-related proteins?

  • Approach: Use assays that measure specific cellular processes affected by the protein, such as actin filament formation or chromatin remodeling.

  • Methods: Quantify changes in these processes upon protein overexpression or depletion.

  • Considerations: Control for potential off-target effects and validate results across multiple experimental conditions.

Given the lack of specific information on Recombinant Drosophila melanogaster Actin-related protein 3 (Arp66B), these FAQs focus on general methodologies and considerations relevant to studying actin-related proteins in Drosophila melanogaster. For detailed research findings on specific proteins, consulting recent scientific literature and databases is recommended.

Example Data Table: Genetic Variation in Recombination Rates

Chromosomal IntervalRecombination Rate Variation
X Chromosome (33 cM)~2-fold among DGRP lines
Chromosome 3R (20.4 cM)~2-fold among DGRP lines

This table illustrates the variation in recombination rates observed in Drosophila melanogaster for different chromosomal intervals, highlighting the genetic basis of such variation .

Detailed Research Findings

Recent studies have identified several genes contributing to natural variation in recombination rates in Drosophila melanogaster, including CG10864, CG33970, Eip75B, lola, and Ptp61F . These findings underscore the complex genetic architecture underlying recombination rate variation and highlight the importance of considering multiple genetic factors in experimental designs.

For actin-related proteins, research has shown that Arp53D plays a critical role in germline-specific actin structures and is required for optimal embryonic development . This demonstrates how specific actin-related proteins can have specialized functions distinct from canonical actin.

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