EGR2 anticorps (AA 1-257)

N° du produit ABIN7599174

Cet anticorps anti-EGR2 est un anticorps Lapin Polyclonal détectant EGR2 dans WB, ELISA et FACS. Adapté pour Humain, Souris et Rat.

Aperçu rapide pour EGR2 anticorps (AA 1-257) (ABIN7599174)

Antigène: EGR2 (Early Growth Response 2 (EGR2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp EGR2 est non-conjugé

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Détail du produit anti-EGR2 anticorps

Épitope: AA 1-257

Fonction: Anti-EGR2 Antibody

Attributs du produit: Anti-EGR2 Antibody (ABIN7599174). Tested in WB, Flow Cytometry, ELISA applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human EGR2 recombinant protein (Position: M1-R257). Human EGR2 shares 90.7% amino acid (aa) sequence identity with both mouse and rat EGR2.

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human
ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Détails sur EGR2

Antigène: EGR2 (Early Growth Response 2 (EGR2))

Autre désignation: EGR2

Sujet: Early growth response protein 2 is a protein that in humans is encoded by the EGR2 gene. The protein encoded by this gene is a transcription factor with three tandem C2H2-type zinc fingers. Defects in this gene are associated with Charcot-Marie-Tooth disease type 1D (CMT1D), Charcot-Marie-Tooth disease type 4E (CMT4E), and with Dejerine-Sottas syndrome (DSS). Multiple transcript variants encoding two different isoforms have been found for this gene.

Poids moléculaire: 50 kDa

ID gène: 1959

UniProt: P11161