GORAB Antikörper (AA 201-300) (AbBy Fluor® 555)
-
- Target Alle GORAB Antikörper anzeigen
- GORAB (Golgin, RAB6-Interacting (GORAB))
-
Bindungsspezifität
- AA 201-300
-
Reaktivität
- Human
-
Wirt
- Kaninchen
-
Klonalität
- Polyklonal
-
Konjugat
- Dieser GORAB Antikörper ist konjugiert mit AbBy Fluor® 555
-
Applikation
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Kreuzreaktivität
- Human
- Homologie
- Mouse,Rat,Dog,Cow,Pig,Horse,Chicken,Rabbit
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human SCYL1BP1
- Isotyp
- IgG
- Top Product
- Discover our top product GORAB Primärantikörper
-
-
- Applikationshinweise
-
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- 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
-
- Target
- GORAB (Golgin, RAB6-Interacting (GORAB))
- Andere Bezeichnung
- SCYL1BP1 (GORAB Produkte)
- Synonyme
- GO antikoerper, NTKLBP1 antikoerper, SCYL1BP1 antikoerper, AI467484 antikoerper, NTKL-BP1 antikoerper, Scyl1bp1 antikoerper, golgin, RAB6 interacting antikoerper, golgin, RAB6-interacting antikoerper, GORAB antikoerper, Gorab antikoerper
- Hintergrund
-
Synonyms: GO, NTKLBP1, SCYL1BP1, RAB6-interacting golgin, N-terminal kinase-like-binding protein 1, NTKL-BP1, NTKL-binding protein 1, hNTKL-BP1, SCY1-like 1-binding protein 1, SCYL1-BP1, SCYL1-binding protein 1, GORAB
Background: Defects in GORAB are the cause of geroderma osteodysplasticum (GO) [MIM:231070], also known as gerodermia osteodysplastica or Walt Disney dwarfism. GO is a rare autosomal recessive disorder characterized by lax, wrinkled skin, joint laxity and a typical face with a prematurely aged appearance. Skeletal signs include severe osteoporosis leading to frequent fractures, malar and mandibular hypoplasia and a variable degree of growth retardation.
- Gen-ID
- 92344
- UniProt
- Q5T7V8
-