GFAP anticorps

N° du produit ABIN659067

Cet anticorps anti-GFAP est un anticorps Souris Monoclonal détectant GFAP dans WB, IF et IHC (p). Adapté pour Humain. Ce Primary Antibody a été cité dans 1 publication.

Aperçu rapide pour GFAP anticorps (ABIN659067)

Antigène: GFAP (Glial Fibrillary Acidic Protein (GFAP))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp GFAP est non-conjugé

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

Clone: 183CT3-1-5

Détail du produit anti-GFAP anticorps

Purification: This antibody is purified through a protein G column, followed by dialysis against PBS.

Immunogène: This GFAP monoclonal antibody is generated from mouse immunized with GFAP recombinant protein.

Isotype: IgG2b kappa

Information d'application

Indications d'application: IF: 1:10~50. WB: 1:4000. WB: 1:100~500. IHC-P-Leica: 1:1000. IHC: 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified monoclonal antibody 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: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Références pour anticorps anti-GFAP (ABIN659067)

Bajpai, Kerosuo, Tseropoulos, Cummings, Wang, Lei, Liu, Liu, Popescu, Bronner, Andreadis: "Reprogramming Postnatal Human Epidermal Keratinocytes Toward Functional Neural Crest Fates." dans: Stem cells (Dayton, Ohio), Vol. 35, Issue 5, pp. 1402-1415, (2018) (PubMed).

Détails sur GFAP

Antigène: GFAP (Glial Fibrillary Acidic Protein (GFAP))

Autre désignation: GFAP

Sujet: This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Poids moléculaire: 49880

ID gène: 2670

NCBI Accession: NP_001124491, NP_001229305, NP_002046

UniProt: P14136