Recombinant Human ANKRD13D, GST-tagged
Cat.No. : | ANKRD13D-9665H |
Product Overview : | Recombinant Human ANKRD13D protein, fused to GST-tag, was expressed in E.coli and purified by GSH-sepharose. |
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Source : | E.coli |
Species : | Human |
Tag : | GST |
Protein length : | 284-367a.a. |
Storage : | The protein is stored in PBS buffer at -20℃. Avoid repeated freezing and thawing cycles. |
Storage Buffer : | 1M PBS (58mM Na2HPO4,17mM NaH2PO4, 68mM NaCl, pH8. ) added with 100mM GSH and 1% Triton X-100,15%glycerol. |
Gene Name : | ANKRD13D ankyrin repeat domain 13 family, member D [ Homo sapiens ] |
Official Symbol : | ANKRD13D |
Synonyms : | ANKRD13D; ankyrin repeat domain 13 family, member D; ankyrin repeat domain-containing protein 13D; MGC50828; |
Gene ID : | 338692 |
mRNA Refseq : | NM_207354 |
Protein Refseq : | NP_997237 |
UniProt ID : | Q6ZTN6 |
Chromosome Location : | 11q13.2 |
Products Types
◆ Recombinant Protein | ||
ANKRD13D-575H | Recombinant Human ANKRD13D protein, GST-tagged | +Inquiry |
◆ Lysates | ||
ANKRD13D-8856HCL | Recombinant Human ANKRD13D 293 Cell Lysate | +Inquiry |
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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (8)
Ask a questionThe tissue-specific expression and developmental regulation of ANKRD13D have not been extensively characterized. Further studies, such as gene expression profiling, could provide insights into its expression patterns.
The post-translational modifications of ANKRD13D have not been well-studied. It is possible that it undergoes various modifications such as phosphorylation, ubiquitination, or acetylation, but further research is needed to understand its post-translational modification profile.
Currently, there are no known functional domains or motifs identified in ANKRD13D. Further investigations and bioinformatic analyses may provide insights into its potential functional regions.
The interaction partners or binding partners of ANKRD13D have not been characterized. Further studies such as protein-protein interaction assays may provide insights into its potential molecular interactions.
There are currently no established links between ANKRD13D and specific signaling pathways. Further studies, such as protein-protein interaction network analyses, may reveal its potential involvement in signaling cascades.
Given the lack of functional characterization, specific cellular processes in which ANKRD13D may be involved are still unknown. Further research is needed to determine its potential roles in cellular activities.
The presence of genetic variations or mutations specifically associated with ANKRD13D has not been well-documented. Future studies, such as genetic association studies, could uncover any potential disease-related variants.
The presence of orthologs or paralogs of ANKRD13D across species has not been extensively investigated. Comparative genomics and phylogenetic analyses could shed light on its evolutionary relationships.
Customer Reviews (5)
Write a reviewthe ANKRD13D protein's quality and suitability for experimental needs, combined with the manufacturer's excellent technical support, create a valuable partnership that enhances research outcomes.
This level of support saves researchers time and resources, enabling them to focus on the scientific aspects of their work and accelerate the overall progress of their studies.
The manufacturer's commitment to excellence is evident through their provision of excellent technical support, which can prove vital in troubleshooting any experimental challenges or addressing specific research questions related to the protein.
Their expertise can help troubleshoot problems, suggest alternative approaches, or provide recommendations for optimizing experimental protocols.
Researchers can feel confident in the reliability and efficacy of the ANKRD13D protein and rely on the manufacturer's expertise to navigate any challenges that may arise during their trials.
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