CMSS1 anticorps (AbBy Fluor® 750)

N° du produit ABIN4998444

Détail du produit anti-CMSS1 anticorps (AbBy Fluor® 750)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CMSS1 est conjugé à/à la AbBy Fluor® 750

Application: Western Blotting (WB)

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: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur CMSS1

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

Autre désignation: C3orf26 (CMSS1 Produits)

Synonymes: anticorps C3orf26, anticorps 1110001A06Rik, anticorps 2610528E23Rik, anticorps 4930572F24Rik, anticorps AV099812, anticorps AV122629, anticorps RGD1309437, anticorps c3orf26, anticorps C1H3orf26, anticorps cms1 ribosomal small subunit homolog (yeast), anticorps cms small ribosomal subunit 1, anticorps cms1 ribosomal small subunit homolog L homeolog, anticorps CMSS1, anticorps Cmss1, anticorps cmss1.L

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.