BZW2 anticorps (FITC)

N° du produit ABIN1400240

Détail du produit anti-BZW2 anticorps (FITC)

Antigène: BZW2 (Basic Leucine Zipper and W2 Domains 2 (BZW2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BZW2 est conjugé à/à la FITC

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human BZW2

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur BZW2

Antigène: BZW2 (Basic Leucine Zipper and W2 Domains 2 (BZW2))

Autre désignation: BZW2 (BZW2 Produits)

Synonymes: anticorps HSPC028, anticorps MGC84347, anticorps MST017, anticorps MSTP017, anticorps 1110001I24Rik, anticorps Bdm2, anticorps Hfb2, anticorps zgc:55580, anticorps basic leucine zipper and W2 domains 2, anticorps basic leucine zipper and W2 domains 2 L homeolog, anticorps BZW2, anticorps bzw2.L, anticorps Bzw2, anticorps bzw2

Sujet:

Synonyms: HSPC028, MSTP017 antibody Basic leucine zipper and W2 domain containing protein 2, Basic leucine zipper and W2 domains 2, BZW 2, MST017, BZW2_HUMAN.

Background: BZW2, also known as HSPC028 or MSTP017, is a 419 amino acid protein that contains one W2 domain and is thought to be involved in neuronal differentiation. The gene encoding BZW2 maps to human chromosome 7. Chromosome 7 houses over 1,000 genes and comprises nearly 5 % of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders, including cases of acute myelogenous leukemia and myelodysplasia.

ID gène: 28969

Pathways: SARS-CoV-2 Protein Interactome