C20orf112 anticorps (AbBy Fluor® 555)
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- Antigène Tous les produits C20orf112 (C20ORF112)
- C20orf112 (C20ORF112) (Chromosome 20 Open Reading Frame 112 (C20ORF112))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp C20orf112 est conjugé à/à la AbBy Fluor® 555
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human C20orf112
- Isotype
- IgG
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- Indications d'application
- IF(IHC-P) 1:50-200
- Restrictions
- For Research Use only
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- 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.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- C20orf112 (C20ORF112) (Chromosome 20 Open Reading Frame 112 (C20ORF112))
- Autre désignation
- C20orf112 (C20ORF112 Produits)
- Synonymes
- anticorps C20orf113, anticorps dJ1184F4.2, anticorps dJ1184F4.4, anticorps nucleolar protein 4 like, anticorps NOL4L
- Sujet
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Synonyms: C20orf112, C20orf113, Chromosome 20 open reading frame 112, CT112_HUMAN, Hypothetical protein LOC140688, Uncharacterized protein C20orf112.
Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf112 gene product has been provisionally designated C20orf112 pending further characterization.
- ID gène
- 140688
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