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FZD4, Blocking Peptide

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产品名称: FZD4, Blocking Peptide
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简单介绍

FZD4, Blocking Peptide


FZD4, Blocking Peptide  的详细介绍
Product Name

FZD4, Blocking Peptide

Full Product Name

FZD4 Immunizing Peptide

Product Synonym Names
FZD4; frizzled homolog 4 (Drosophila); CD344; EVR1; FEVR; FZD4S; Fz-4; FzE4; GPCR; MGC34390; WNT receptor frizzled-4; exudative vitreoretinopathy 1 (autosomal dominant; Criswick-Schepens syndrome); frizzled 4
Product Gene Name

FZD4 blocking peptide

[Similar Products]
Antibody/Peptide Pairs
FZD4 peptide (MBS428060) is used for blocking the activity of FZD4 antibody (MBS423263)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Sequence
C-KIRSNLQK DGTKT
OMIM
133780
Species Reactivity
Human, Mouse, Rat
Form/Format
100ug of dried peptide
Preparation and Storage
Shipped at ambient temperature, store at -20 degree C
ISO Certification
Manufactured in an ISO 9001:2008 Certified Laboratory.
Other Notes
Small volumes of FZD4 blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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NCBI/Uniprot data below describe general gene information for FZD4. It may not necessarily be applicable to this product.
NCBI GI #
22547161
NCBI GeneID
8322
NCBI Accession #
NP_036325.2 [Other Products]
NCBI GenBank Nucleotide #
NM_012193.3 [Other Products]
UniProt Secondary Accession #
Q14C97; Q6S9E4; A8K9Q3[Other Products]
UniProt Related Accession #
Q9ULV1[Other Products]
Molecular Weight
59,881 Da
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NCBI Official Full Name
frizzled-4
NCBI Official Synonym Full Names
frizzled class receptor 4
NCBI Official Symbol
FZD4  [Similar Products]
NCBI Official Synonym Symbols
Fz4; EVR1; FEVR; Fz-4; FzE4; GPCR; hFz4; CD344; FZD4S
  [Similar Products]
NCBI Protein Information
frizzled-4
UniProt Protein Name
Frizzled-4
UniProt Synonym Protein Names
FzE4; CD_antigen: CD344
UniProt Gene Name
FZD4  [Similar Products]
UniProt Synonym Gene Names
Fz-4; hFz4  [Similar Products]
UniProt Entry Name
FZD4_HUMAN
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NCBI Summary for FZD4
This gene is a member of the frizzled gene family. Members of this family encode seven-transmembrane domain proteins that are receptors for the Wingless type MMTV integration site family of signaling proteins. Most frizzled receptors are coupled to the beta-catenin canonical signaling pathway. This protein may play a role as a positive regulator of the Wingless type MMTV integration site signaling pathway. A transcript variant retaining intronic sequence and encoding a shorter isoform has been described, however, its expression is not supported by other experimental evidence. [provided by RefSeq, Jul 2008]
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UniProt Comments for FZD4
FZD4: Receptor for Wnt proteins. Most of frizzled receptors are coupled to the beta-catenin (CTNNB1) canonical signaling pathway, which leads to the activation of disheveled proteins, inhibition of GSK-3 kinase, nuclear accumulation of beta-catenin (CTNNB1) and activation of Wnt target genes. Plays a critical role in retinal vascularization by acting as a receptor for Wnt proteins and norrin (NDP). In retina, it can be both activated by Wnt protein-binding, but also by a Wnt-independent signaling via binding of norrin (NDP), promoting in both cases beta-catenin (CTNNB1) accumulation and stimulation of LEF/TCF-mediated transcriptional programs. A second signaling pathway involving PKC and calcium fluxes has been seen for some family members, but it is not yet clear if it represents a distinct pathway or if it can be integrated in the canonical pathway, as PKC seems to be required for Wnt-mediated inactivation of GSK-3 kinase. Both pathways seem to involve interactions with G-proteins. May be involved in transduction and intercellular transmission of polarity information during tissue morphogenesis and/or in differentiated tissues. Defects in FZD4 are the cause of vitreoretinopathy exudative type 1 (EVR1); also known as autosomal dominant familial exudative vitreoretinopathy (FEVR) or Criswick- Schepens syndrome. EVR1 is a disorder of the retinal vasculature characterized by an abrupt cessation of growth of peripheral capillaries, leading to an avascular peripheral retina. This may lead to compensatory retinal neovascularization, which is thought to be induced by hypoxia from the initial avascular insult. New vessels are prone to leakage and rupture causing exudates and bleeding, followed by scarring, retinal detachment and blindness. Clinical features can be highly variable, even within the same family. Patients with mild forms of the disease are asymptomatic, and their only disease-related abnormality is an arc of avascular retina in the extreme temporal periphery. Belongs to the G-protein coupled receptor Fz/Smo family.

Protein type: Receptor, GPCR; GPCR, Fz/Smo family; Membrane protein, integral; Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 11q14.2

Cellular Component: cell surface; integral to membrane; integral to plasma membrane; intercellular junction; plasma membrane

Molecular Function: cytokine binding; G-protein coupled receptor activity; PDZ domain binding; protein binding; protein heterodimerization activity; protein homodimerization activity; ubiquitin protein ligase binding; Wnt receptor activity; Wnt-protein binding

Biological Process: G-protein coupled receptor protein signaling pathway; locomotion during locomotory behavior; neuron differentiation; positive regulation of JNK activity; positive regulation of transcription factor activity; positive regulation of transcription, DNA-dependent; progesterone secretion; regulation of vascular endothelial growth factor receptor signaling pathway; sensory perception of sound; vasculogenesis; Wnt receptor signaling pathway; Wnt receptor signaling pathway through beta-catenin; Wnt receptor signaling pathway, calcium modulating pathway; Wnt receptor signaling pathway, planar cell polarity pathway

Disease: Exudative Vitreoretinopathy 1
Research Articles on FZD4
1. These structural, biophysical and cellular data, map Fz4 and putative Lrp5/6 s to distinct patches on Norrin, and reveal a GAG spanning Norrin and Fz4 cysteine-rich domain.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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