TTPA anticorps (AA 82-108)

N° du produit ABIN5537880

Détail du produit anti-TTPA anticorps

Antigène: TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))

Épitope: AA 82-108

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TTPA est non-conjugé

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This TTPA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 82-108 amino acids from the Central region of human TTPA.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Stockage commentaire: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur TTPA

Antigène: TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))

Autre désignation: TTPA (TTPA Produits)

Synonymes: anticorps ATTP, anticorps AVED, anticorps TTP1, anticorps alphaTTP, anticorps TTP, anticorps alpha-TTP, anticorps alpha tocopherol transfer protein, anticorps tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency), anticorps tocopherol (alpha) transfer protein, anticorps TTPA, anticorps ttpa, anticorps Ttpa

Sujet: This gene encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. This protein plays an important role in regulating vitamin E levels in the body by transporting vitamin E between membrane vesicles and facilitating the secretion of vitamin E from hepatocytes to circulating lipoproteins. Mutations in this gene cause hereditary vitamin E deficiency (ataxia with vitamin E deficiency, AVED) and retinitis pigmentosa.

Poids moléculaire: 32 kDa

ID gène: 7274

UniProt: P49638