NDE1 Antikörper
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- Target Alle NDE1 Antikörper anzeigen
- NDE1
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser NDE1 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)
- Immunogen
- nudE nuclear distribution gene E homolog 1 (A. nidulans)
- Isotyp
- IgG
- Top Product
- Discover our top product NDE1 Primärantikörper
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- Applikationshinweise
- Optimal working dilution should be determined by the investigator.
- Kommentare
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A2780 cells were subjected to SDS PAGE followed by western blot with FNab05600(NDE1 antibody) at dilution of 1:1500
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Buffer
- PBS with 0.02 % sodium azide and 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.
- Handhabung
- Avoid repeated freeze / thaw cycles.
- Lagerung
- -20 °C
- Haltbarkeit
- 12 months
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- Target
- NDE1
- Andere Bezeichnung
- NDE1 (NDE1 Produkte)
- Synonyme
- 2810027M15Rik antikoerper, AU042936 antikoerper, AW822251 antikoerper, Nude antikoerper, mNudE antikoerper, HOM-TES-87 antikoerper, LIS4 antikoerper, NDE antikoerper, NUDE antikoerper, NUDE1 antikoerper, fb82g01 antikoerper, im:7141877 antikoerper, wu:fb82g01 antikoerper, zgc:114109 antikoerper, nudE neurodevelopment protein 1 antikoerper, Nde1 antikoerper, NDE1 antikoerper, nde1 antikoerper
- Hintergrund
- Synonyms:NUDE Background:This gene encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe mental retardation. Alternative splicing results in multiple transcript variants.
- Molekulargewicht
- 40 kDa
- Gen-ID
- 54820
- UniProt
- Q9NXR1
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