WNT7A Antikörper
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- Target Alle WNT7A Antikörper anzeigen
- WNT7A (Wingless-Type MMTV Integration Site Family, Member 7A (WNT7A))
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Reaktivität
- Human, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser WNT7A Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunofluorescence (IF)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human WNT7A (NP_004616.2).
- Isotyp
- IgG
- Top Product
- Discover our top product WNT7A Primärantikörper
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- Applikationshinweise
- WB 1:500-1:2000 IF 1:10-1:100
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- 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
- WNT7A (Wingless-Type MMTV Integration Site Family, Member 7A (WNT7A))
- Andere Bezeichnung
- WNT7A (WNT7A Produkte)
- Synonyme
- wnt7a antikoerper, AI849442 antikoerper, Wnt-7a antikoerper, px antikoerper, tw antikoerper, Xwnt-7a antikoerper, wnt-7a antikoerper, wnt7a-A antikoerper, Wnt family member 7A antikoerper, wingless-type MMTV integration site family, member 7Aa antikoerper, wingless-type MMTV integration site family, member 7A antikoerper, wingless-type MMTV integration site family member 7A S homeolog antikoerper, WNT7A antikoerper, wnt7aa antikoerper, Wnt7a antikoerper, wnt7a.S antikoerper
- Hintergrund
- This gene is a member of the WNT gene family, which consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is involved in the development of the anterior-posterior axis in the female reproductive tract, and also plays a critical role in uterine smooth muscle pattering and maintenance of adult uterine function. Mutations in this gene are associated with Fuhrmann and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromes.
- Molekulargewicht
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Observed_MW: 39 kDa
Calculated_MW: 39 kDa
- Gen-ID
- 7476
- UniProt
- O00755
- Pathways
- WNT Signalweg, Stem Cell Maintenance, Asymmetric Protein Localization
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