C3orf39 antibody
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- Target See all C3orf39 (GTDC2) Antibodies
- C3orf39 (GTDC2) (Glycosyltransferase-Like Domain Containing 2 (GTDC2))
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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 C3orf39 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 C3orf39
- Isotype
- IgG
- Top Product
- Discover our top product GTDC2 Primary Antibody
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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
- C3orf39 (GTDC2) (Glycosyltransferase-Like Domain Containing 2 (GTDC2))
- Alternative Name
- C3orf39 (GTDC2 Products)
- Synonyms
- AGO61 antibody, C3orf39 antibody, GTDC2 antibody, C22H3orf39 antibody, C23H3orf39 antibody, ago61 antibody, Ago61 antibody, C85492 antibody, RGD1304827 antibody, MDDGA8 antibody, protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) antibody, protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2 antibody, POMGNT2 antibody, Pomgnt2 antibody
- Background
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Synonyms: AGO61, Chromosome 3 open reading frame 39, FLJ14566, Uncharacterized glycosyltransferase AGO61 precursor, GTDC2_HUMAN.
Background: C3orf39, also known as AGO61, is a 580 amino acid secreted protein belonging to the glycosyltransferase 61 family. C3orf39 is encoded by a gene that maps to human chromosome 3p25.1. 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
- 84892
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