FZD9 Antikörper (AA 469-591)
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- Target Alle FZD9 Antikörper anzeigen
- FZD9 (Frizzled Family Receptor 9 (FZD9))
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Bindungsspezifität
- AA 469-591
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser FZD9 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunofluorescence (IF)
- Sequenz
- ERLNMDFWRL RATEQPCAAA AGPGGRRDCS LPGGSVPTVA VFMLKIFMSL VVGITSGVWV WSSKTFQTWQ SLCYRKIAAG RARAKACRAP GSYGRGTHCH YKAPTVVLHM TKTDPSLENP THL
- Kreuzreaktivität
- Human, Maus, Ratte
- Produktmerkmale
- Polyclonal Antibodies
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 469-591 of human FZD9 (NP_003499.1).
- Isotyp
- IgG
- Top Product
- Discover our top product FZD9 Primärantikörper
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- Applikationshinweise
- WB,1:500 - 1:2000,IF,1:50 - 1:100
- Kommentare
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HIGH QUALITY
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- FZD9 (Frizzled Family Receptor 9 (FZD9))
- Andere Bezeichnung
- FZD9 (FZD9 Produkte)
- Synonyme
- CD349 antikoerper, FZD3 antikoerper, mfz9 antikoerper, Fz-9 antikoerper, cFz-9 antikoerper, fz11 antikoerper, fzd9 antikoerper, fzx antikoerper, hm:zehl0603 antikoerper, zehl0603 antikoerper, zg11 antikoerper, frizzled class receptor 9 antikoerper, frizzled class receptor 9a antikoerper, frizzled class receptor 9b antikoerper, FZD9 antikoerper, Fzd9 antikoerper, fzd9a antikoerper, fzd9b antikoerper
- Hintergrund
- Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney.,FZD9,CD349,FZD3,Epigenetics & Nuclear Signaling,Translation Control,Regulation of eIF4 and p70 S6 Kinase,Signal Transduction,G protein signaling,G-Protein-Coupled Receptors(GPCR),mTOR Signaling Pathway,Cell Biology & Developmental Biology,Wnt/β-Catenin Signaling Pathway,ESC Pluripotency and Differentiation,Immunology & Inflammation,CD markers,Neuroscience,Stem Cells,Neural Stem Cells,FZD9
- Molekulargewicht
- 64 kDa
- Gen-ID
- 8326
- UniProt
- O00144
- Pathways
- WNT Signalweg
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