Metabolism Antibodies 1
Anti-DVL1 Antibody (CAB10536)
- SKU:
- CAB10536
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Metabolism
Description
Antibody Name: | Anti-DVL1 Antibody |
Antibody SKU: | CAB10536 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IHC IF |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 510-640 of human DVL1 (NP_004412.2). |
Application: | WB IHC IF |
Recommended Dilution: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | Mouse kidney |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 510-640 of human DVL1 (NP_004412.2). |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | GQGY PYQY PGPP PCFP PAYQ DPGF SYGS GSTG SQQS EGSK SSGS TRSS RRAP GREK ERRA AGAG GSGS ESDH TAPS GVGS SWRE RPAG QLSR GSSP RSQA SATA PGLP PPHP TTKA YTVV GGPP GGPP VRE |
Gene ID: | 1855 |
Uniprot: | O14640 |
Cellular Location: | Cell membrane, Cytoplasm, Cytoplasmic side, Cytoplasmic vesicle, Peripheral membrane protein, cytosol |
Calculated MW: | 72kDa/75kDa |
Observed MW: | 72kDa |
Synonyms: | DVL1, DRS2, DVL, DVL1L1, DVL1P1 |
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. |
UniProt Protein Function: | DVL1: 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). Belongs to the DSH family. 2 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:Inhibitor Chromosomal Location of Human Ortholog: 1p36 Cellular Component: cytoplasmic membrane-bound vesicle; cytoplasmic vesicle; cytosol; growth cone; lateral plasma membrane; neuron projection; synapse Molecular Function:enzyme binding; frizzled binding; identical protein binding; protein binding; protein kinase binding Biological Process: dendrite morphogenesis; negative regulation of protein binding; negative regulation of protein kinase activity; neural tube development; neuromuscular junction development; neurotransmitter secretion; positive regulation of proteasomal ubiquitin-dependent protein catabolic process; positive regulation of transcription, DNA-dependent; positive regulation of Wnt receptor signaling pathway; protein stabilization; receptor clustering; regulation of neurotransmitter levels; synapse organization and biogenesis; synaptogenesis; transcription from RNA polymerase II promoter; Wnt receptor signaling pathway through beta-catenin; Wnt receptor signaling pathway, planar cell polarity pathway Disease: Robinow Syndrome, Autosomal Dominant; Robinow Syndrome, Autosomal Dominant 2 |
NCBI Summary: | 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] |
UniProt Code: | O14640 |
NCBI GenInfo Identifier: | 145559469 |
NCBI Gene ID: | 1855 |
NCBI Accession: | O14640.2 |
UniProt Secondary Accession: | O14640,Q5TA33, Q5TA35, |
UniProt Related Accession: | P54792,O14640 |
Molecular Weight: | 72,881 Da |
NCBI Full Name: | Segment polarity protein dishevelled homolog DVL-1 |
NCBI Synonym Full Names: | dishevelled segment polarity protein 1 |
NCBI Official Symbol: | DVL1 |
NCBI Official Synonym Symbols: | DVL; DRS2; DVL1L1; DVL1P1 |
NCBI Protein Information: | segment polarity protein dishevelled homolog DVL-1 |
UniProt Protein Name: | Segment polarity protein dishevelled homolog DVL-1 |
UniProt Synonym Protein Names: | DSH homolog 1 |
Protein Family: | Segment polarity protein dishevelled |
UniProt Gene Name: | DVL1 |
UniProt Entry Name: | DVL1_HUMAN |