SCXA anticorps (full length)

N° du produit ABIN7878978

L’anticorps anti-SCXA Monoclonal Souris est utilisé pour la détection de SCXA dans des échantillons de Humain. Il a été validé pour FACS et IF.

Aperçu rapide pour SCXA anticorps (full length) (ABIN7878978)

Antigène: SCXA (Scleraxis (SCXA))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp SCXA est non-conjugé

Application: Flow Cytometry (FACS), Immunofluorescence (IF)

Classe de qualité: Carrier-free

Clone: PCRP-SCXA-1D2

Détail du produit anti-SCXA anticorps

Épitope: full length

Fonction: Scleraxis Antibody / SCXA (azide and preservative free)

Purification: Protein A/G affinity

Immunogène: Recombinant full-length human SCXA protein was used as the immunogen for the Scleraxis antibody.

Isotype: IgG2a

Information d'application

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

Détails sur SCXA

Antigène: SCXA (Scleraxis (SCXA))

Autre désignation: Scleraxis

Sujet: Transcription factors are proteins that bind DNA adjacent to genes and control the production of mRNA transcripts. Scleraxis (basic helix-loop-helix transcription factor scleraxis) is a 201 amino acid protein that dimerizes with another bHLH protein to initiate transcription. Scleraxis is known to play a role in formation of mesoderm and somite-derived chondrogenic lineages. Scleraxis localizes to the nucleus and contains one bHLH domain. bHLH transcription factors, in general, function in cellular differentiation, proliferation, and oncogene regulation. The gene encoding Scleraxis maps to human chromosome 8, which consists of nearly 146 million base pairs, houses more than 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: Q7RTU7