LZTR1 anticorps (N-Term)

N° du produit ABIN6991281

Cet anticorps anti-LZTR1 est un anticorps Lapin Polyclonal détectant LZTR1 dans WB, ELISA et IHC (p). Adapté pour Humain, Souris et Rat.

Aperçu rapide pour LZTR1 anticorps (N-Term) (ABIN6991281)

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), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-LZTR1 anticorps

Épitope: AA 130-180, N-Term

Purification: LZTR1 Antibody is affinity chromatography purified via peptide column.

Immunogène: LZTR1 antibody was raised against a 14 amino acid synthetic peptide near the amino terminus of human LZTR1. The immunogen is located within amino acids 130 - 180 of LZTR1.

Isotype: IgG

Information d'application

Indications d'application: LZTR1 antibody can be used for detection of LZTR1 by Western blot at 1 - 2 μ,g/mL. Antibody can also be used for immunohistochemistry starting at 5 μ,g/mL.

Antibody validated: Western Blot in human samples and Immunohistochemistry in mouse samples. All other applications and species not yet tested.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: LZTR1 Antibody is supplied in 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.

Stock: -20 °C,4 °C

Stockage commentaire: LZTR1 antibody can be stored 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 LZTR1

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

Autre désignation: LZTR1

Sujet: LZTR1 Antibody: 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.

ID gène: 8216

UniProt: Q8N653