C21ORF56 antibody (Biotin)
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- Target See all C21ORF56 (C21orf56) products
- C21ORF56 (C21orf56) (Chromosome 21 Open Reading Frame 56 (C21orf56))
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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 C21ORF56 antibody is conjugated to Biotin
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Cross-Reactivity
- Human, Mouse, Rat
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C21ORF56
- Isotype
- IgG
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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
- C21ORF56 (C21orf56) (Chromosome 21 Open Reading Frame 56 (C21orf56))
- Alternative Name
- C21ORF56 (C21orf56 Products)
- Synonyms
- C21orf56 antibody, spermatogenesis and centriole associated 1 like antibody, SPATC1L antibody
- Background
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Synonyms: Chromosome 21 open reading frame 56, DKFZp434N0650, MGC99490, Uncharacterized protein C21orf56, SPC1L_HUMAN.
Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf56 gene product has been provisionally designated C21orf56 pending further characterization.
- Gene ID
- 84221
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