BATF3 anticorps (AA 1-123)

N° du produit ABIN7868023

Cet anticorps anti-BATF3 Monoclonal Souris (Clone PCRP-BATF3-1E5) (ABIN7868023) détecte spécifiquement BATF3 dans IHC (p) et FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour BATF3 anticorps (AA 1-123) (ABIN7868023)

Antigène: BATF3 (Basic Leucine Zipper Transcriptional Factor ATF-Like 3 (BATF3))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp BATF3 est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Clone: PCRP-BATF3-1E5

Détail du produit anti-BATF3 anticorps

Épitope: AA 1-123

Fonction: SNFT Antibody / BATF3

Purification: Protein A/G affinity

Immunogène: A recombinant partial protein sequence (within amino acids 1-123) from the human protein was used as the immunogen for the SNFT antibody.

Isotype: IgG1, kappa

Information d'application

Indications d'application: Optimal dilution of the SNFT antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.2 mg/mL

Buffer: 0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % 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

Stockage commentaire: Aliquot the SNFT antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur BATF3

Antigène: BATF3 (Basic Leucine Zipper Transcriptional Factor ATF-Like 3 (BATF3))

Autre désignation: SNFT

Sujet: SNFT, also known as BATF3 (basic leucine zipper transcription factor, ATF-like 3), JUNDM1 or JDP1, is a 127 amino acid protein that localizes to the nucleus and contains one bZIP domain. Interacting with c-Jun, SNFT functions as a negative regulator of AP-1-mediated transcription, specifically by heterodimerizing with c-Jun and binding to DNA response elements. The gene encoding SNFT maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

UniProt: Q9NR55