DLX3 Antikörper
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- Target Alle DLX3 Antikörper anzeigen
- DLX3 (Distal-Less Homeobox 3 (DLX3))
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Monoklonal
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Konjugat
- Dieser DLX3 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Verwendungszweck
- DLX3 Rabbit mAb
- Kreuzreaktivität
- Human, Maus
- Produktmerkmale
- Monoclonal Antibodies
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of Human DLX3.
- Isotyp
- IgG
- Top Product
- Discover our top product DLX3 Primärantikörper
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- Applikationshinweise
- WB,1:500 - 1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,0.05 % BSA,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
- DLX3 (Distal-Less Homeobox 3 (DLX3))
- Andere Bezeichnung
- DLX3 (DLX3 Produkte)
- Synonyme
- AI4 antikoerper, TDO antikoerper, AV237891 antikoerper, Dlx-3 antikoerper, DLX3 antikoerper, ai4 antikoerper, tdo antikoerper, xdlx3 antikoerper, MGC69301 antikoerper, dll2 antikoerper, dlx3 antikoerper, dlx-3 antikoerper, id:ibd3531 antikoerper, wu:fb83f11 antikoerper, zgc:91827 antikoerper, distal-less homeobox 3 antikoerper, distal-less homeobox 3 L homeolog antikoerper, distal-less homeobox 3b antikoerper, DLX3 antikoerper, Dlx3 antikoerper, dlx3 antikoerper, dlx3.L antikoerper, dlx3b antikoerper
- Hintergrund
- Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism.,DLX3,AI4,TDO,Epigenetics & Nuclear Signaling,Transcription Factors,DLX3
- Molekulargewicht
- 31kDa
- Gen-ID
- 1747
- UniProt
- O60479
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