HLCS anticorps (AA 14-654)

N° du produit ABIN7825287

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

Aperçu rapide pour HLCS anticorps (AA 14-654) (ABIN7825287)

Antigène: HLCS (Biotin-Protein Ligase (HLCS))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HLCS est non-conjugé

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (IHC)

Détail du produit anti-HLCS anticorps

Épitope: AA 14-654

Fonction: Anti-HLCS Antibody

Réactivité croisée (Details): No cross-reactivity with other proteins

Homologie: Human HLCS shares 75.9% amino acid (aa) sequence identity with mouse HLCS.

Attributs du produit: Anti-HLCS Antibody. Tested in WB, IHC, Flow Cytometry, ELISA applications. This antibody reacts with Human, Mouse, Rat.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human HLCS recombinant protein (Position: Q14-K654). Human HLCS shares 75.9% amino acid (aa) sequence identity with mouse HLCS.

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Rat Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human ELISA, 0.1-0.5 μg/mL

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur HLCS

Antigène: HLCS (Biotin-Protein Ligase (HLCS))

Autre désignation: HLCS

Sujet:

Background: This gene encodes an enzyme that catalyzes the binding of biotin to carboxylases and histones. The protein plays an important role in gluconeogenesis, fatty acid synthesis and branched chain amino acid catabolism. Defects in this gene are the cause of holocarboxylase synthetase deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified.

Gene Full Name: holocarboxylase synthetase

Poids moléculaire: 81 kDa

ID gène: 3141

UniProt: P50747