ARG58502

anti-DVL1 / Dishevelled 1 antibody

anti-DVL1 / Dishevelled 1 antibody for ICC/IF,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse,Rat

Overview

Product Description Rabbit Polyclonal antibody recognizes DVL1 / Dishevelled 1
Tested Reactivity Hu, Ms, Rat
Tested Application ICC/IF, IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name DVL1 / Dishevelled 1
Antigen Species Human
Immunogen Recombinant fusion protein corresponding to aa. 510-640 of Human DVL1 / Dishevelled 1 (NP_004412.2).
Conjugation Un-conjugated
Alternate Names DVL; DSH homolog 1; DVL1P1; DVL1L1; DRS2; Segment polarity protein dishevelled homolog DVL-1; Dishevelled-1

Application Instructions

Application Suggestion
Tested Application Dilution
ICC/IF1:50 - 1:200
IHC-P1:50 - 1:200
WB1:500 - 1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control Mouse heart
Observed Size 90 kDa

Properties

Form Liquid
Purification Affinity purified.
Buffer PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol.
Preservative 0.02% Sodium azide
Stabilizer 50% Glycerol
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 13542 Mouse DVL1

GeneID: 1855 Human DVL1

GeneID: 83721 Rat DVL1

Gene Symbol DVL1
Gene Full Name dishevelled segment polarity protein 1
Background DVL1, the human homolog of the Drosophila dishevelled gene (dsh) encodes a cytoplasmic phosphoprotein that regulates cell proliferation, acting as a transducer molecule for developmental processes, including segmentation and neuroblast specification. DVL1 is a candidate gene for neuroblastomatous transformation. The Schwartz-Jampel syndrome and Charcot-Marie-Tooth disease type 2A have been mapped to the same region as DVL1. The phenotypes of these diseases may be consistent with defects which might be expected from aberrant expression of a DVL gene during development. [provided by RefSeq, Jul 2008]
Function Participates in Wnt signaling by binding to the cytoplasmic C-terminus of frizzled family members and transducing the Wnt signal to down-stream effectors. Plays a role both in canonical and non-canonical Wnt signaling. Plays a role in the signal transduction pathways mediated by multiple Wnt genes. Required for LEF1 activation upon WNT1 and WNT3A signaling. DVL1 and PAK1 form a ternary complex with MUSK which is important for MUSK-dependent regulation of AChR clustering during the formation of the neuromuscular junction (NMJ). [UniProt]
Cellular Localization Cell membrane, Peripheral membrane protein, Cytoplasmic side, Cytoplasm, cytosol, Cytoplasmic vesicle. [UniProt]
Calculated MW 75 kDa
PTM Ubiquitinated; undergoes both 'Lys-48'-linked ubiquitination, leading to its subsequent degradation by the ubiquitin-proteasome pathway, and 'Lys-63'-linked ubiquitination. The interaction with INVS is required for ubiquitination. Deubiquitinated by CYLD, which acts on 'Lys-63'-linked ubiquitin chains (By similarity). [UniProt]

Images (1) Click the Picture to Zoom In

  • ARG58502 anti-DVL1 / Dishevelled 1 antibody WB image

    Western blot: 25 µg of Mouse heart lysate stained with ARG58502 anti-DVL1 / Dishevelled 1 antibody at 1:1000 dilution.