C18orf56 antibody (Biotin)
Quick Overview for C18orf56 antibody (Biotin) (ABIN1404019)
Target
Reactivity
Host
Clonality
Conjugate
Application
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Cross-Reactivity
- Human
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Purification
- Purified by Protein A.
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Immunogen
- KLH conjugated synthetic peptide derived from human C18orf56
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Isotype
- IgG
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anti-Chromosome 18 Open Reading Frame 56 (C18orf56) (N-Term) antibody
C18orf56 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
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Application Notes
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WB 1:300-5000
IHC-P 1:200-400 -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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Preservative
- ProClin
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Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Store at -20°C for 12 months.
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Expiry Date
- 12 months
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- C18orf56 (Chromosome 18 Open Reading Frame 56 (C18orf56))
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Alternative Name
- C18orf56
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Background
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Synonyms: Putative uncharacterized protein C18orf56, CR056_HUMAN.
Background: Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF_ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.
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Gene ID
- 494514
Target
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