C21orf62 antibody
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- Target See all C21orf62 products
- C21orf62 (Chromosome 21 Open Reading Frame 62 (C21orf62))
- Reactivity
- Human, Rat, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C21orf62 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 C21ORF62
- Isotype
- IgG
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anti-Chromosome 21 Open Reading Frame 62 (C21orf62) (AA 108-157) antibody
C21orf62 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
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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
- C21orf62 (Chromosome 21 Open Reading Frame 62 (C21orf62))
- Alternative Name
- C21ORF62 (C21orf62 Products)
- Synonyms
- B37 antibody, PRED81 antibody, C21orf120 antibody, MGC88933 antibody, chromosome 21 open reading frame 62 antibody, chromosome 1 open reading frame, human C21orf62 antibody, chromosome 3 open reading frame, human C21orf62 antibody, C21orf62 antibody, C1H21ORF62 antibody, c21orf62 antibody, C3H21orf62 antibody
- Background
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Synonyms: B37, C21orf120, Chromosome 21 open reading frame 62, Hypothetical protein LOC56245, PRED81, Uncharacterized protein C21orf62, CU062_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 C21orf62 gene product has been provisionally designated C21orf62 pending further characterization.
- Gene ID
- 56245
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