Chromosome 15 Open Reading Frame 58 (C15orf58) (AA 301-385) Antikörper (FITC)

Produktnummer ABIN1710651

Produktdetails

Target: Chromosome 15 Open Reading Frame 58 (C15orf58)

Bindungsspezifität: AA 301-385

Reaktivität: Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: FITC

Applikation: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Kreuzreaktivität: Maus, Ratte

Homologie: Human,Pig,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GDPGP1/C15orf58

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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

Antigendetails

Target: Chromosome 15 Open Reading Frame 58 (C15orf58)

Andere Bezeichnung: GDPGP1/C15orf58 (C15orf58 Produkte)

Synonyme: C15orf58 antikoerper, VTC2 antikoerper, D330012F22Rik antikoerper, C21H15orf58 antikoerper, c15orf58 antikoerper, GDP-D-glucose phosphorylase 1 antikoerper, GDP-D-glucose phosphorylase 1 S homeolog antikoerper, GDPGP1 antikoerper, Gdpgp1 antikoerper, gdpgp1.S antikoerper

Hintergrund:

Synonyms: C15orf58, Chromosome 15 open reading frame 58, GDP-D-glucose phosphorylase 1, GDP-D-glucose phosphorylase C15orf58, gdpgp1, GDPP1_HUMAN, VTC2.

Background: Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.

Gen-ID: 390637