MANSC1 anticorps (AA 21-337) (Fluoro550)

N° du produit ABIN8007783

L’anticorps anti-MANSC1 Polyclonal Lapin est utilisé pour la détection de MANSC1 dans des échantillons de Humain. Il a été validé pour FACS.

Aperçu rapide pour MANSC1 anticorps (AA 21-337) (Fluoro550) (ABIN8007783)

Antigène: MANSC1 (MANSC Domain Containing 1 (MANSC1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MANSC1 est conjugé à/à la Fluoro550

Application: Flow Cytometry (FACS)

Détail du produit anti-MANSC1 anticorps (Fluoro550)

Épitope: AA 21-337

Fonction: Anti-MANSC1 Antibody Fluoro550 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human MANSC1 recombinant protein (Position: L21-N337).

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur MANSC1

Antigène: MANSC1 (MANSC Domain Containing 1 (MANSC1))

Autre désignation: MANSC1

Sujet:

Background: MANSC1 (MANSC domain-containing protein 1), also known as LOH12CR3 (Loss of heterozygosity 12 chromosomal region 3 protein), is a 414 amino acid single-pass membrane protein. Expressed throughout the body, MANSC1 contains one MANSC domain and is encoded by a gene that is located on chromosome 12. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction.

Gene Full Name: MANSC domain containing 1

ID gène: 54682

UniProt: Q9H8J5