ACP6 anticorps

N° du produit ABIN7241639

Détail du produit anti-ACP6 anticorps

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACP6 est non-conjugé

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

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant protein of human ACP6

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000, IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.2 mg/mL

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur ACP6

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

Autre désignation: ACP6 (ACP6 Produits)

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

Sujet: 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.

Poids moléculaire: 49 kDa

UniProt: Q9NPH0