LZTR1 anticorps (N-Term)

N° du produit ABIN500210

L’anticorps Lapin Polyclonal anti-LZTR1 a été validé pour WB, IHC (p) et EIA. Il convient pour détecter LZTR1 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour LZTR1 anticorps (N-Term) (ABIN500210)

Antigène: LZTR1 (Leucine-Zipper-Like Transcription Regulator 1 (LZTR1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LZTR1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Détail du produit anti-LZTR1 anticorps

Épitope: N-Term

Réactivité croisée (Details): Species reactivity (tested):Human, mouse, rat

Purification: Peptide affinity chromatography

Immunogène: LZTR1 antibody was raised against a 14 amino acid peptide near the amino terminus of human LZTR1.

Isotype: IgG

Information d'application

Indications d'application: ELISA. Western blot: 1 - 2 μg/mL. Immunohistochemistry on paraffin sections.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Concentration: 1.0 mg/mL

Buffer: PBS containing 0.02 % 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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: -20 °C

Stockage commentaire: Store the antibody (in aliquots) at -20 °C.

Détails sur LZTR1

Antigène: LZTR1 (Leucine-Zipper-Like Transcription Regulator 1 (LZTR1))

Autre désignation: LZTR1

Sujet: LZTR1, a member of the BTB-kelch superfamily, was initially described as a putative transcriptional regulator based on weak homology to members of the basic leucine zipper-like family, the encoded protein subsequently has been shown to localize exclusively to the Golgi network where it may help stabilize the Golgi complex. Deletion of this gene may be associated with DiGeorge syndrome, a developmental field defect involving the third and fourth pharyngeal pouches, causing the absence of thymus and parathyroid glands, congenital cardiac abnormalities and facial dysmorphism. LZTR1 is tyrosine phosphorylated and subsequently degraded upon induction of apoptosis.Synonyms: Leucine zipper-like transcription regulator 1

ID gène: 8216

UniProt: Q20WK0