Recombinant Macaca fascicularis Cadherin 6(CDH6),partial (Active)

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Code CSB-MP4958MOV
Abbreviation Recombinant Cynomolgus monkey CDH6 protein, partial (Active)
MSDS
Size $114
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  • (Tris-Glycine gel) Discontinuous SDS-PAGE (reduced) with 5% enrichment gel and 15% separation gel.
  • Activity
    Measured by its binding ability in a functional ELISA. Immobilized Macaca fascicularis CDH6 at 2μg/mL can bind Anti-CDH6 recombinant antibody (CSB-RA005055MA1HU),the EC50 is 2.076-2.371 ng/mL. Biological Activity Assay
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Product Details

Purity
Greater than 95% as determined by SEC-HPLC.
Endotoxin
Less than 1.0 EU/ug as determined by LAL method.
Activity
Measured by its binding ability in a functional ELISA. Immobilized Macaca fascicularis CDH6 at 2 μg/mL can bind Anti-CDH6 recombinant antibody (CSB-RA005055MA1HU). The EC50 is 2.076-2.371 ng/mL.
Target Names
Uniprot No.
Species
Macaca fascicularis (Crab-eating macaque) (Cynomolgus monkey)
Source
Mammalian cell
Expression Region
22-614aa
Target Protein Sequence
TPLSKRTSGFPAKKRALELSGNSKNELSRSKRSWMWNQFFLLEEYTGSDYQYVGKLHSDQDRGDGSLKYILSGDGAGDLFIINENTGDIQATKRLDREEKPVYILRAQAINRRTGRPVEPESEFIIKIHDINDNEPIFTKEVYTATVPEMSDVGTFVVQVTATDADDPTYGNSAKVVYSILQGQPYFSVESETGIIKTALLNMDRENREQYQVVIQAKDMGGQMGGLSGTTTVNITLTDVNDNPPRFPQSTYQFKTPESSPPGTPIGRIKASDADVGENAEIEYSITDGEGLDMFDVITDQETQEGIITVKKLLDFEKKKVYTLKVEASNPHVEPRFLYLGPFKDSATVRIVVEDVDEPPVFSKLAYILQIREDAQINTTIGSVTAQDPDAARNPVKYSVDRHTDMDRIFNIDSGNGSIFTSKLLDRETLLWHNITVIATEINNPKQSSRVPLYIKVLDVNDNAPEFAEFYETFVCEKAKADQLIQTLRAVDKDDPYSGHQFSFSLAPEAASGSNFTIQDNKDNTAGILTRKNGYNRHEMSTYLLPVVISDNDYPVQSSTGTVTVRVCACDHHGNMQSCHAEALIHPTGLSTG
Mol. Weight
67.4 kDa
Protein Length
Partial
Tag Info
C-terminal 10xHis-tagged
Form
Lyophilized powder
Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
Buffer
Lyophilized from a 0.2 μm sterile filtered 20 mM Tris-HCl, 0.5 M NaCl, 6% Trehalose, pH 8.0
Reconstitution
We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
Troubleshooting and FAQs
Storage Condition
Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
Shelf Life
The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
Lead Time
3-7 business days
Notes
Repeated freezing and thawing is not recommended. Store working aliquots at 4℃ for up to one week.
Datasheet & COA
Please contact us to get it.
Description

The recombinant Macaca fascicularis CDH6 protein is an active, high-purity product designed for functional studies. It is expressed in mammalian cells, ensuring proper folding and post-translational modifications. The construct includes amino acids 22 to 614 of the native CDH6 protein, with a C-terminal 10xHis tag to aid in purification and detection. This recombinant CDH6 protein is supplied as a lyophilized powder and shows greater than 95% purity, as verified by SEC-HPLC. Endotoxin levels are strictly controlled, measuring below 1.0 EU/µg, confirmed using the LAL assay. Its biological activity is validated through a functional ELISA: when immobilized at 2 μg/mL, it effectively binds the anti-CDH6 recombinant antibody (CSB-RA005055MA1HU), with an EC50 ranging between 2.076 and 2.371 ng/mL, demonstrating reliable binding performance.

The protein CDH6 is a member of the cadherin family that plays a significant role in neural development and tissue architecture. In the context of Macaca fascicularis, also known as the cynomolgus monkey, the exploration of CDH6 addresses its implications in neurogenesis and structural connectivity within the central nervous system.

Cadherins, including CDH6, are crucial for mediating cell-cell adhesion, particularly in the brain, where they facilitate the organization of neural circuits by maintaining synaptic integrity. For instance, the expression of CDH6 has been identified in specific regions of the brain associated with sensory processing, which may reflect its role in the establishment and maintenance of synaptic connections that are vital for proper sensory integration and cognitive functions [1][2]. Specifically, CDH6 expression patterns can indicate its involvement in the architectural configuration of the cerebral cortex and its connections, as observed through investigations into the neuroanatomy of primate species [2][3].

Beyond structural contributions, CDH6 is implicated in the modulation of developmental processes, which may influence behavioral outcomes. Given that Macaca fascicularis serves as a model organism for studying human neurological conditions, understanding CDH6's function may provide insights into the underlying genetic mechanisms linked to neural disorders. Research involving various cadherin family members shows that alterations in their expression can lead to dysregulation in neural development, which is pertinent to both normal and pathological states of neurodevelopment [4][5].

Furthermore, studies into gene expression across species indicate that cadherin genes, including CDH6, undergo evolutionary conservation, highlighting their fundamental role across primate species [6][7]. This reflects a broader trend within primate phylogenomics, where gene flow and adaptive evolutionary traits often underscore the relevance of certain genes in physiological adaptations and constraints [8][9].

References:
[1] L. Ramsay, M. Quillé, et al. Blood transcriptomic biomarker as a surrogate of ischemic brain gene expression. Annals of Clinical and Translational Neurology, vol. 6, no. 9, p. 1681-1695, 2019. https://doi.org/10.1002/acn3.50861
[2] L. Zhuo, M. Wang, et al. Mapbrain: a multi-omics atlas of the primate brain. Nucleic Acids Research, vol. 53, no. D1, p. D1055-D1065, 2024. https://doi.org/10.1093/nar/gkae911
[3] A. Goulas, P. Majka, M. Rosa, & C. Hilgetag. A blueprint of mammalian cortical connectomes. Plos Biology, vol. 17, no. 3, p. e2005346, 2019. https://doi.org/10.1371/journal.pbio.2005346
[4] E. Takahashi, J. Saruwatari, T. Fujimoto, Y. Tanoue, T. Fukuda, & T. Inoue. The effects of exosomes derived from trabecular meshwork cells on schlemm’s canal endothelial cells. Scientific Reports, vol. 11, no. 1, 2021. https://doi.org/10.1038/s41598-021-01450-9
[5] E. Robertson, S. Boehnke, et al. Comparison of cerebrospinal fluid biomarkers relevant to neurodegenerative diseases in healthy cynomolgus and rhesus macaque monkeys. 2021. https://doi.org/10.1101/2021.03.01.433384
[6] N. Galtier. An approximate likelihood method reveals ancient gene flow between human, chimpanzee and gorilla. 2023. https://doi.org/10.1101/2023.07.06.547897
[7] D. Vanderpool, B. Minh, et al. Primate phylogenomics uncovers multiple rapid radiations and ancient interspecific introgression. Plos Biology, vol. 18, no. 12, p. e3000954, 2020. https://doi.org/10.1371/journal.pbio.3000954
[8] S. Seehase, H. Lauenstein, et al. Lps-induced lung inflammation in marmoset monkeys – an acute model for anti-inflammatory drug testing. Plos One, vol. 7, no. 8, p. e43709, 2012. https://doi.org/10.1371/journal.pone.0043709
[9] S. Mariya, F. Dewi, et al. Isolation and characterization of c-c chemokine ligand 7 (ccl7) in cynomolgus macaques. Hayati Journal of Biosciences, vol. 26, no. 3, p. 129, 2019. https://doi.org/10.4308/hjb.26.3.129

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