LHPP anticorps (AA 6-270)

N° du produit ABIN7875947

Cet anticorps Lapin Polyclonal détecte spécifiquement LHPP dans WB, ELISA, IF et FACS. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour LHPP anticorps (AA 6-270) (ABIN7875947)

Antigène: LHPP (Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LHPP est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)

Détail du produit anti-LHPP anticorps

Épitope: AA 6-270

Fonction: LHPP Antibody / Phospholysine phosphohistidine inorganic pyrophosphate phosphatase

Purification: Antigen affinity purified

Immunogène: An E.coli-derived human recombinant protein (amino acids K6-K270) was used as the immunogen for the LHPP antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the LHPP antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the LHPP antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur LHPP

Antigène: LHPP (Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP))

Autre désignation: LHPP

Sujet: LHPP, also known as HDHD2B, is a 270 amino acid protein that exists as a homodimer and is a member of the HAD-like hydrolase superfamily. Expressed in liver, kidney and moderately in brain, LHPP is encoded by a gene located on 10, which houses over 1,200 genes and comprises nearly 4.5 % of the human genome. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria

UniProt: Q9H008