CSF3R anticorps (AA 25-622)

N° du produit ABIN7092971

Cet anticorps anti-CSF3R Monoclonal Lapin (Clone DM172) (ABIN7092971) détecte spécifiquement CSF3R dans ELISA et FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour CSF3R anticorps (AA 25-622) (ABIN7092971)

Antigène: CSF3R (Colony Stimulating Factor 3 Receptor (Granulocyte) (CSF3R))

Reactivité: Humain

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp CSF3R est non-conjugé

Application: ELISA, Flow Cytometry (FACS)

Clone: DM172

Détail du produit anti-CSF3R anticorps

Épitope: AA 25-622

Fonction: Anti-CD114 antibody(DM172), Rabbit mAb

Purification: Purified from cell culture supernatant by affinity chromatography

Immunogène: Recombinant human CD114(Glu25-Pro622) (ABIN6961136) produced by using human HEK293 cells

Isotype: IgG

Information d'application

Indications d'application: ELISA 1:5000-10000, Flow Cyt 1:100

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Please see Certificate of Analysis for specific instructions of reconstitution.

Buffer: Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

Stock: -20 °C,-80 °C

Stockage commentaire: Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

Date de péremption: 12 months

Détails sur CSF3R

Antigène: CSF3R (Colony Stimulating Factor 3 Receptor (Granulocyte) (CSF3R))

Autre désignation: CD114

Sujet: Synonyms:CSF3R,CD114,GCSFR
Description:The protein encoded by this gene is the receptor for colony stimulating factor 3, a cytokine that controls the production, differentiation, and function of granulocytes. The encoded protein, which is a member of the family of cytokine receptors, may also function in some cell surface adhesion or recognition processes. Alternatively spliced transcript variants have been described. Mutations in this gene are a cause of Kostmann syndrome, also known as severe congenital neutropenia.

Poids moléculaire: 92.2KDa

UniProt: Q99062