ACP6 Antikörper

Produktnummer ABIN7241639

Produktdetails anti-ACP6 Antikörper

Target: ACP6 (Acid Phosphatase 6, Lysophosphatidic (ACP6))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ACP6 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human ACP6

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000, IHC 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.2 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu ACP6

Target: ACP6 (Acid Phosphatase 6, Lysophosphatidic (ACP6))

Andere Bezeichnung: ACP6 (ACP6 Produkte)

Synonyme: ACP6 antikoerper, im:7147584 antikoerper, zgc:172268 antikoerper, MGC146066 antikoerper, ACPL1 antikoerper, LPAP antikoerper, PACPL1 antikoerper, 5730559A09Rik antikoerper, AU022842 antikoerper, mPACPL1 antikoerper, acid phosphatase 6, lysophosphatidic antikoerper, acid phosphatase 6, lysophosphatidic S homeolog antikoerper, ACP6 antikoerper, acp6 antikoerper, acp6.S antikoerper, Acp6 antikoerper

Hintergrund: Lysophosphatidic acid phosphatase type 6 (ACP6), also designated acid phosphatase-like protein 1 (ACPL1) or lysophosphatidic acid phosphatase (LPAP), is a 428 amino acid secreted protein that hydrolyzes lysophosphatidic acid to monoacylglycerol. ACP6 is highly expressed in kidney, heart, small intestine, muscle, liver, prostate, testis, ovary and exists as two isoforms as a result of alternative splicing events. The gene encoding ACP6 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene of human chromosome 1, which encodes lamin A. Stickler syndrome, Parkinsons, Gaucher disease, familial adenomatous polyposis and Usher syndrome are also associated with chromosome 1. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

Molekulargewicht: 49 kDa

UniProt: Q9NPH0