C3orf49 antibody (Biotin)
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- Target See all C3orf49 products
- C3orf49 (Chromosome 3 Open Reading Frame 49 (C3orf49))
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C3orf49 antibody is conjugated to Biotin
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Cross-Reactivity
- Human
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C3orf49
- Isotype
- IgG
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anti-Chromosome 3 Open Reading Frame 49 (C3orf49) (AA 1-292) antibody
C3orf49 Reactivity: Human WB, ELISA Host: Rabbit Polyclonal unconjugated
anti-Chromosome 3 Open Reading Frame 49 (C3orf49) (Middle Region) antibodyC3orf49 Reactivity: Human, Rat, Cow, Dog, Horse, Rabbit 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
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
- Storage Comment
- Store at -20°C for 12 months.
- Expiry Date
- 12 months
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- Target
- C3orf49 (Chromosome 3 Open Reading Frame 49 (C3orf49))
- Alternative Name
- C3orf49 (C3orf49 Products)
- Synonyms
- chromosome 3 open reading frame 49 antibody, C3orf49 antibody
- Background
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Synonyms: chromosome 3 open reading frame 49, MGC17310, CC049_HUMAN.
Background: C3orf49 is a 292 amino acid protein encoded by a gene that maps to human chromosome 3p14.1. 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
- 132200
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