C3orf18 antibody
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- Target See all C3orf18 products
- C3orf18 (Chromosome 3 Open Reading Frame 18 (C3orf18))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C3orf18 antibody is un-conjugated
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Cross-Reactivity
- Human, Mouse, Rat
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C3orf18
- Isotype
- IgG
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- Application Notes
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- 4 °C,-20 °C
- Storage Comment
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Expiry Date
- 12 months
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- Target
- C3orf18 (Chromosome 3 Open Reading Frame 18 (C3orf18))
- Alternative Name
- C3orf18 (C3orf18 Products)
- Synonyms
- G20 antibody, chromosome 3 open reading frame 18 antibody, chromosome 12 C3orf18 homolog antibody, chromosome 2 open reading frame, human C3orf18 antibody, C3orf18 antibody, C12H3orf18 antibody, C2H3orf18 antibody
- Background
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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.
- Gene ID
- 51161
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