BATF3 anticorps (AA 1-123)

N° du produit ABIN7868022

L’anticorps anti-BATF3 Monoclonal Souris est utilisé pour la détection de BATF3 dans des échantillons de Humain. Il a été validé pour IHC (p) et FACS.

Aperçu rapide pour BATF3 anticorps (AA 1-123) (ABIN7868022)

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)

Classe de qualité: Carrier-free

Clone: PCRP-BATF3-1E5

Détail du produit anti-BATF3 anticorps

Épitope: AA 1-123

Fonction: SNFT Antibody / BATF3 (azide and preservative free)

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: 1 mg/mL

Buffer: 1 mg/mL in 1X PBS, BSA free, sodium azide free

Agent conservateur: Azide free

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