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Mouse Anti-WDFY3 Recombinant Antibody (CBYY-1609) (CBMAB-1680-YY)

This product is mouse antibody that recognizes WDFY3. The antibody CBYY-1609 can be used for immunoassay techniques such as: ELISA, WB
See all WDFY3 antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
CBYY-1609
Antibody Isotype
IgG1, κ
Application
ELISA, WB

Basic Information

Immunogen
WDFY3 (AAH15214, 1 a.a. ~ 420 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.Immunogen sequence: MGTSKEKAKT ATLKQALLGH TDTVTCATAS LAYHIIVSGS RDRTCIIWDL NKLSFLTQLR GHRAPVSALC INELTGDIVS CAGTYIHVWS INGNPIVSVN TFTGRSQQII CCCMouseEMNEW DTQNVIVTGH SDGVVRFWRM EFLQVPETPA PEPAEVLEMQ EDCPEAQIGQ EAQDEDSSDS EADEQSISQD PKDTPSQPSS TSHRPRAASC RATAAWCTDS GSDDSRRWSD QLSLDEKDGF IFVNYSEGQT RAHLQGPLSH PHPNPIEVRN YSRLKPGYRW ERQLVFRSKL TMHTAFDRKD NAHPAEVTAL GISKDHSRIL VGDSRGRVFS WSVSDQPGRS AADHWVKDEG GDSCSGCSVR FSLTERRHHC RNCGQLFCQK CSRFQSEIKR LKISSPVRVC QNCYYNLQHE RGSEDGPRNC
Specificity
Human
Antibody Isotype
IgG1, κ
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
WD repeat and FYVE domain containing 3
Introduction
This gene encodes a phosphatidylinositol 3-phosphate-binding protein that functions as a master conductor for aggregate clearance by autophagy. This protein shuttles from the nuclear membrane to colocalize with aggregated proteins, where it complexes with other autophagic components to achieve macroautophagy-mediated clearance of these aggregated proteins. However, it is not necessary for starvation-induced macroautophagy.
Entrez Gene ID
23001
UniProt ID
Q8IZQ1
Alternative Names
WD Repeat And FYVE Domain Containing 3; Autophagy-Linked FYVE Protein; ALFY; WD Repeat And FYVE Domain-Containing Protein 3; KIAA0993; ZFYVE25; MCPH18; BCHS;
Function
Required for selective macroautophagy (aggrephagy). Acts as an adapter protein by linking specific proteins destined for degradation to the core autophagic machinery members, such as the ATG5-ATG12-ATG16L E3-like ligase, SQSTM1 and LC3 (PubMed:20417604).
Along with p62/SQSTM1, involved in the formation and autophagic degradation of cytoplasmic ubiquitin-containing inclusions (p62 bodies, ALIS/aggresome-like induced structures). Along with SQSTM1, required to recruit ubiquitinated proteins to PML bodies in the nucleus (PubMed:20168092).
Important for normal brain development. Essential for the formation of axonal tracts throughout the brain and spinal cord, including the formation of the major forebrain commissures. Involved in the ability of neural cells to respond to guidance cues. Required for cortical neurons to respond to the trophic effects of netrin-1/NTN1 (By similarity).
Regulates Wnt signaling through the removal of DVL3 aggregates, likely in an autophagy-dependent manner. This process may be important for the determination of brain size during embryonic development (PubMed:27008544).
May regulate osteoclastogenesis by acting on the TNFSF11/RANKL - TRAF6 pathway (By similarity).
After cytokinetic abscission, involved in midbody remnant degradation (PubMed:24128730).
In vitro strongly binds to phosphatidylinositol 3-phosphate (PtdIns3P) (PubMed:15292400).
Biological Process
Biological Process aggrephagy Source:UniProtKB1 Publication
Cellular Location
Nucleus membrane
Cytoplasm, cytosol
Nucleus, PML body
Membrane
Perikaryon
Cell projection, axon
Relocalization from the nucleus to the cytosol is stimulated by cellular stress, such as starvation or proteasomal inhibition. In the cytosol of starved cells, colocalizes with autophagic structures (PubMed:15292400, PubMed:20168092, PubMed:20971078, PubMed:20417604).
This redistribution is dependent on p62/SQSTM1 (PubMed:20168092).
When nuclear export is blocked by treatment with leptomycin B, accumulates in nuclear bodies, that completely or partially colocalize with promyelocytic leukemia (PML) bodies (PubMed:20168092).
Localizes throughout neurons, including within axons. In neurons, enriched in the light membrane fraction along with the synaptosomal membrane protein synaptophysin and the membrane-bound form of LC3/MAP1LC3A/MAP1LC3B, called LC3-II, a classic marker for autophagic vesicles (By similarity).
Involvement in disease
Microcephaly 18, primary, autosomal dominant (MCPH18):
A form of microcephaly, a disease defined as a head circumference more than 3 standard deviations below the age, sex and ethnically matched mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. MCPH18 affected individuals manifest microcephaly with mild to moderate intellectual disability.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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