CMSS1 anticorps (AA 101-200)

N° du produit ABIN1713725

L’anticorps Lapin Polyclonal anti-CMSS1 a été validé pour WB et ELISA. Il convient pour détecter CMSS1 dans des échantillons de Humain.

Aperçu rapide pour CMSS1 anticorps (AA 101-200) (ABIN1713725)

Antigène: CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CMSS1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-CMSS1 anticorps

Épitope: AA 101-200

Réactivité croisée: Humain

Homologie: Mouse,Rat,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C3orf26

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur CMSS1

Antigène: CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))

Autre désignation: C3orf26

Sujet:

Synonyms: C3orf26, CC026_HUMAN, MGC4308, Uncharacterized protein C3orf26.

Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The C3orf26 gene product has been provisionally designated C3orf26 pending further characterization.