Frizzled-4 rabbit pAb

Frizzled-4 rabbit pAb

AO-06-ES7665-100

Frizzled-4 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES7665
Product nameFrizzled-4 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsIF;ELISA
Other nameFZD4; Frizzled-4; Fz-4; hFz4; FzE4; CD antigen CD344
Size100μL
Unit price ($)248
Human gene ID8322
Human Swiss-ProtQ9ULV1
SourceRabbit
IsotypeIgG
TargetFrizzled-4
Fields>>mTOR signaling pathway;>>Wnt signaling pathway;>>Hippo signaling pathway;>>Signaling pathways regulating pluripotency of stem cells;>>Melanogenesis;>>Cushing syndrome;>>Alzheimer disease;>>Pathways of neurodegeneration - multiple diseases;>>Human papillomavirus infection;>>Pathways in cancer;>>Proteoglycans in cancer;>>Basal cell carcinoma;>>Breast cancer;>>Hepatocellular carcinoma;>>Gastric cancer
Gene nameFZD4
Protein nameFrizzled-4
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID14366
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ61088
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID64558
Rat gene linkView Rat Gene
Rat Swiss-ProtQ9QZH0
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human FZD4. AA range:131-180
SpecificityFrizzled-4 Polyclonal Antibody detects endogenous levels of Frizzled-4 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionImmunofluorescence: 1/200 - 1/1000. ELISA: 1/5000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)60kD
Observed band (KD)
Backgroundfrizzled class receptor 4(FZD4) Homo sapiens 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],
Functiondisease:Defects in FZD4 are the cause of vitreoretinopathy exudative type 1 (EVR1) [MIM:133780]; 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.,domain:Lys-Thr-X-X-X-Trp mot
Subcellular locationCell membrane ; Multi-pass membrane protein .
ExpressionAlmost ubiquitous (PubMed:10544037). Largely expressed in adult heart, skeletal muscle, ovary, and fetal kidney (PubMed:10544037). Moderate amounts in adult liver, kidney, pancreas, spleen, and fetal lung, and small amounts in placenta, adult lung, prostate, testis, colon, fetal brain and liver (PubMed:10544037).

Additional Images

Image 1
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Immunofluorescence analysis of LOVO cells, using FZD4 Antibody. The picture on the right is blocked with the synthesized peptide.
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: AO-06-ES7665-100
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Hurry! only 10 items left in stock.

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