Mouse anti-Human sapiens (Human) DPYSL5 Monoclonal Antibody
Mouse anti-Human sapiens (Human) DPYSL5 Monoclonal Antibody - Image 2
Mouse anti-Human sapiens (Human) DPYSL5 Monoclonal Antibody - Image 3

Mouse anti-Human sapiens (Human) DPYSL5 Monoclonal Antibody

Mouse anti-Human sapiens (Human) DPYSL5 Monoclonal Antibody — recombinant protein.

SKU: BCREC-000377MA Category:
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Product Specifications

Uniprot No.Q9BPU6
Target NamesDPYSL5
Species ReactivityMouse
ImmunogenRecombinant Human DPYSL5 protein
Immunogen SpeciesHomo sapiens (Human)
ConjugateNon-conjugated
IsotypeMouse IgG1 kappa
ClonalityMonoclonal
ApplicationsELISA, WB, FC, ICC
BufferPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
StorageUpon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Function

Involved in the negative regulation of dendrite outgrowth.

Biological Context

Subcellular Location: Cytoplasm
Disease Association: Ritscher-Schinzel syndrome 4 (RTSC4) : An autosomal dominant form of Ritscher-Schinzel syndrome, a developmental malformation syndrome characterized by cerebellar brain anomalies associated with global developmental delay and impaired intellectual development, congenital heart defects, and craniofacial abnormalities. [The disease is caused by variants affecting the gene represented in this entry]

Product Specifications

Mouse anti-Human sapiens (Human) DPYSL5 Monoclonal Antibody is a recombinant protein. Suitable for ELISA and Western Blot applications.

Applications: ELISA, WB, FC, ICC

Biological Activity: Not implied unless activity data are explicitly listed on this product page, the datasheet, or the CoA.

Storage: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Shipping & Lead Time: Availability, shipping conditions, and estimated lead time are confirmed in the formal quotation or order confirmation based on the product format, destination, and order requirements.

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Protein Biology

Function

Involved in the negative regulation of dendrite outgrowth

Subcellular Location

Cytoplasm

Disease Association

Ritscher-Schinzel syndrome 4 (RTSC4) : An autosomal dominant form of Ritscher-Schinzel syndrome, a developmental malformation syndrome characterized by cerebellar brain anomalies associated with global developmental delay and impaired intellectual development, congenital heart defects, and craniofacial abnormalities. [The disease is caused by variants affecting the gene represented in this entry]

Subunit

Homotetramer, and heterotetramer with other DPYS-like proteins. Interacts with DPYSL2, DPYSL3 and DPYSL4 (By similarity). Interacts with MAP2 and TUBB3 (PubMed:33894126)

Gene: DPYSL5  |  Organism: Homo sapiens  |  Synonyms: CRMP3-associated molecule; Collapsin response mediator protein 5; UNC33-like phosphoprotein 6
Key Publications

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Frequently Asked Questions

How do I order or inquire about this product?

Submit the Online Inquiry form with your required quantity and specifications, or email sales@biocrestsci.com. Available sizes, pricing, stock status, documentation, and estimated lead time are confirmed in the formal quotation.

What is the shipping and delivery time?

Availability, dispatch timing, shipping conditions, and delivery estimates depend on the product format, destination, and order requirements. These details are confirmed in the formal quotation or order confirmation.

How should this product be stored?

Follow the storage and handling instructions in the product-specific datasheet and Certificate of Analysis (CoA). Requirements may vary by product form and formulation; contact BioCrest Sci if product-specific guidance is needed.

What quality controls are performed on your products?

Quality-control data such as identity, purity, endotoxin level, or biological activity are provided only when specified on this product page, the datasheet, or Certificate of Analysis (CoA). Biological activity is not implied unless explicitly stated.

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