NECAB1 anticorps

N° du produit ABIN7881753

Cet anticorps Souris Monoclonal détecte spécifiquement NECAB1 dans WB et IHC (p). Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour NECAB1 anticorps (ABIN7881753)

Antigène: NECAB1 (N-terminal EF-Hand Calcium Binding Protein 1 (NECAB1))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp NECAB1 est non-conjugé

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

Classe de qualité: Carrier-free

Clone: NECAB1-7677

Détail du produit anti-NECAB1 anticorps

Fonction: NECAB1 Antibody / N-terminal EF-hand calcium binding protein 1 (azide and preservative free)

Purification: Protein A/G affinity

Immunogène: Recombinant human NECAB1 protein was used as the immunogen for the NECAB1 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the NECAB1 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 NECAB1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur NECAB1

Antigène: NECAB1 (N-terminal EF-Hand Calcium Binding Protein 1 (NECAB1))

Autre désignation: NECAB1

Sujet: Members of the EF-CBP (N-terminal EF-hand calcium binding protein)/NECAB (neuronal calcium-binding protein) family participate in neuronal calcium signaling. EF-CBP1 (N-terminal EF-hand calcium binding protein 1), also known as STIP-1 or neuronal calcium-binding protein 1 (NECAB1), is a 351 amino acid cytoplasmic protein that contains one antibiotic biosynthesis monooxygenase (ABM) domain and 2 EF-hand domains. Expressed in brain, EF-CBP1 interacts with copine 6 and Syntaxin, and exists as two alternatively spliced isoforms. The gene encoding EF-CBP1 maps to human chromosome 8, which consists of nearly 146 million base pairs, encodes over 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.

UniProt: Q8N987