C3orf18 anticorps (Biotin)
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- Antigène Tous les produits C3orf18
- C3orf18 (Chromosome 3 Open Reading Frame 18 (C3orf18))
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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 C3orf18 est conjugé à/à la Biotin
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human C3orf18
- Isotype
- IgG
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- Indications d'application
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WB 1:300-5000
IHC-P 1:200-400 - 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 for 12 months.
- Date de péremption
- 12 months
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- Antigène
- C3orf18 (Chromosome 3 Open Reading Frame 18 (C3orf18))
- Autre désignation
- C3orf18 (C3orf18 Produits)
- Synonymes
- anticorps G20, anticorps chromosome 3 open reading frame 18, anticorps chromosome 12 C3orf18 homolog, anticorps chromosome 2 open reading frame, human C3orf18, anticorps C3orf18, anticorps C12H3orf18, anticorps C2H3orf18
- Sujet
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Synonyms: C3orf18, CC018_HUMAN, Protein G20, chromosome 3 open reading frame 18, Uncharacterized protein C3orf18.
Background: C3orf18, also known as G20, is a 162 amino acid single pass membrane protein that is encoded by a gene mapping to human chromosome 3q25.3. Chromosome 3 is made up of approximately 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.
- ID gène
- 51161
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