NDE1 Antikörper (AA 1-110)
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- Target Alle NDE1 Antikörper anzeigen
- NDE1
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Bindungsspezifität
- AA 1-110
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Reaktivität
- Human
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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), Immunohistochemistry (IHC)
- Sequenz
- MEDSGKTFSS EEEEANYWKD LAMTYKQRAE NTQEELREFQ EGSREYEAEL ETQLQQIETR NRDLLSENNR LRMELETIKE KFEVQHSEGY RQISALEDDL AQTKAIKDQL
- Kreuzreaktivität
- Human, Maus, Ratte
- Produktmerkmale
- Polyclonal Antibodies
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-110 of human NDE1 (NP_060138.1).
- Isotyp
- IgG
- Top Product
- Discover our top product NDE1 Primärantikörper
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- Applikationshinweise
- WB,1:500 - 1:2000,IHC,1:50 - 1:200
- 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
- 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
- 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.,NDE1,HOM-TES-87,LIS4,MHAC,NDE,NUDE,NUDE1,Epigenetics & Nuclear Signaling,Cell Biology & Developmental Biology,Cell Cycle,Centrosome,Neuroscience,NDE1
- Molekulargewicht
- 37 kDa/38 kDa
- Gen-ID
- 54820
- UniProt
- Q9NXR1
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