C20orf26 antibody (AA 651-750) (Biotin)
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- Target See all C20orf26 (C20ORF26) products
- C20orf26 (C20ORF26) (Chromosome 20 Open Reading Frame 26 (C20ORF26))
- Binding Specificity
- AA 651-750
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C20orf26 antibody is conjugated to Biotin
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Application
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Predicted Reactivity
- Human,Mouse,Rat,Pig,Horse,Rabbit
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C20orf26
- Isotype
- IgG
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- Application Notes
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 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
- C20orf26 (C20ORF26) (Chromosome 20 Open Reading Frame 26 (C20ORF26))
- Alternative Name
- C20orf26 (C20ORF26 Products)
- Synonyms
- dJ1002M8.3 antibody, dJ1178H5.4 antibody, cilia and flagella associated protein 61 antibody, CFAP61 antibody
- Background
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Synonyms: C20orf26, CT026_HUMAN, dJ1002M8.3, dJ1178H5.4, RP11-470C13.3, Uncharacterized protein C20orf26.
Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf26 gene product has been provisionally designated C20orf26 pending further characterization.
- Gene ID
- 26074
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