CCDC22 anticorps (N-Term)

N° du produit ABIN1449944

L’anticorps Lapin Polyclonal anti-CCDC22 a été validé pour WB, IF et EIA. Il convient pour détecter CCDC22 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour CCDC22 anticorps (N-Term) (ABIN1449944)

Antigène: CCDC22 (Coiled-Coil Domain Containing 22 (CCDC22))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CCDC22 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Enzyme Immunoassay (EIA)

Détail du produit anti-CCDC22 anticorps

Épitope: N-Term

Purification: Affinity chromatography purified via peptide column

Immunogène: CCDC22 antibody was raised against an 18 amino acid synthetic peptide near the amino terminus of Human CCDC22

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Concentration: 1.0 mg/mL

Buffer: PBS containing 0.02 % Sodium Azide as preservative

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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur CCDC22

Antigène: CCDC22 (Coiled-Coil Domain Containing 22 (CCDC22))

Autre désignation: CCDC22

Sujet: CCDC22 is a recently identified coiled-coil domain-containing protein that has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. In rat, CCDC22 has been observed to localize in multiple regions of the brain, including the prefrontal and somatosensory cortex, dentate gyrus and thalamus, and in the ipsilateral motor neurons of the spinal cord after sciatic nerve transection suggesting that it may play a role in neuronal injury response. The human CCDC22 gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability (XLID).Synonyms: CXorf37, Coiled-coil domain-containing protein 22

ID gène: 28952

NCBI Accession: NP_054727