PEX19 Antikörper

Produktnummer ABIN6989698

Produktdetails anti-PEX19 Antikörper

Target: PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Monoklonal

Konjugat: Dieser PEX19 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Kreuzreaktivität: Human

Aufreinigung: Purified by Protein A.

Immunogen: Synthetic peptide within N-terminal Human PEX19.

Klon: 9H3

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
FCM 1:20-100
IHC-P 1:200-400

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 1xTBS ( pH 7.4), 1 % BSA, 40 %Glycerol and 0.05 % Sodium Azide.

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 for 12 months.

Haltbarkeit: 12 months

Details zu PEX19

Target: PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

Andere Bezeichnung: PEX19 (PEX19 Produkte)

Synonyme: BEST:GH03076 antikoerper, CG5325 antikoerper, DmelPex19 antikoerper, Dmel\\CG5325 antikoerper, D1S2223E antikoerper, HK33 antikoerper, PBD12A antikoerper, PMP1 antikoerper, PMPI antikoerper, PXF antikoerper, PXMP1 antikoerper, Pxf antikoerper, PxF antikoerper, Peroxin-19 antikoerper, Peroxin 19 antikoerper, Peroxisomal farnesylated protein antikoerper, peroxisomal biogenesis factor 19 antikoerper, Pex19 antikoerper, Bm1_19905 antikoerper, PEX19 antikoerper

Hintergrund:

Synonyms: 33 kDa housekeeping protein antibody, D1S2223E antibody, HK33 antibody, Housekeeping gene 33kD antibody, OK/SW-cl.22 antibody, PBD12A antibody, Peroxin 19 antibody, Peroxin-19 antibody, Peroxisomal biogenesis factor 19 antibody, Peroxisomal farnesylated protein antibody, PEX19 antibody, PEX19_HUMAN antibody, PMP1 antibody, PMPI antibody, PXF antibody, PXMP1 antibody

Background: This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]

Gen-ID: 5824

UniProt: P40855