TCTN2 Antikörper (AA 61-160) (AbBy Fluor® 555)
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- Target Alle TCTN2 Antikörper anzeigen
- TCTN2 (Tectonic Family Member 2 (TCTN2))
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Bindungsspezifität
- AA 61-160
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Reaktivität
- Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser TCTN2 Antikörper ist konjugiert mit AbBy Fluor® 555
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Applikation
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Kreuzreaktivität
- Maus
- Homologie
- Human,Rat
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human TCTN2
- Isotyp
- IgG
- Top Product
- Discover our top product TCTN2 Primärantikörper
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- Applikationshinweise
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- TCTN2 (Tectonic Family Member 2 (TCTN2))
- Andere Bezeichnung
- TCTN2 (TCTN2 Produkte)
- Synonyme
- fb44f11 antikoerper, wu:fb44f11 antikoerper, tect2 antikoerper, C12orf38 antikoerper, MKS8 antikoerper, TECT2 antikoerper, 4432405B04Rik antikoerper, Tect2 antikoerper, tectonic family member 2 antikoerper, TCTN2 antikoerper, tctn2 antikoerper, Tctn2 antikoerper
- Hintergrund
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Synonyms: C12orf38, FLJ12975, MKS8, OTTHUMP00000239215, OTTHUMP00000239216, Tctn2, TECT2, TECT2_HUMAN, Tectonic family member 2, Tectonic-2.
Background: Defects in TCTN2 are the cause of Meckel syndrome type 8 (MKS8) [MIM:613885]. A disorder characterized by a combination of renal cysts and variably associated features including developmental anomalies of the central nervous system (typically encephalocele), hepatic ductal dysplasia and cysts, and polydactyly.
- Pathways
- Proton Transport
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