DPCR1 Antikörper (Cy3)

Produktnummer ABIN1418453

Der Kaninchen Polyklonal Anti-DPCR1-Antikörper wurde für WB und IF (p) validiert. Er ist geeignet, DPCR1 in Proben von Human zu detektieren.

Kurzübersicht für DPCR1 Antikörper (Cy3) (ABIN1418453)

Target: DPCR1 (Diffuse Panbronchiolitis Critical Region 1 (DPCR1))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DPCR1 Antikörper ist konjugiert mit Cy3

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

Produktdetails anti-DPCR1 Antikörper (Cy3)

Kreuzreaktivität: Human

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human DPCR1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 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

Details zu DPCR1

Target: DPCR1 (Diffuse Panbronchiolitis Critical Region 1 (DPCR1))

Andere Bezeichnung: DPCR1

Hintergrund:

Synonyms: Dfuse panbronchiolitis critical region 1, Dfuse panbronchiolitis critical region, Dfuse panbronchiolitis critical region protein 1, DKFZp666O235, DPCR protein, MGC126710, MGC126712, OTTHUMP00000062447, PBLT, bCX105N19.6, DPCR1_HUMAN.

Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6.

Gen-ID: 135656