FAM207A antibody (AA 95-120) (AbBy Fluor® 488)
Quick Overview for FAM207A antibody (AA 95-120) (AbBy Fluor® 488) (ABIN1405744)
Target
Reactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 95-120
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Cross-Reactivity
- Human
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Purification
- Purified by Protein A.
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Immunogen
- KLH conjugated synthetic peptide derived from human C21orf70
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Isotype
- IgG
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anti-Family with Sequence Similarity 207, Member A (FAM207A) (AA 95-120) antibody
FAM207A Reactivity: Human IF (p), IHC (p) Host: Rabbit Polyclonal unconjugated
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Application Notes
- IF(IHC-P) 1:50-200
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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Preservative
- ProClin
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Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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Expiry Date
- 12 months
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- FAM207A (Family with Sequence Similarity 207, Member A (FAM207A))
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Alternative Name
- C21orf70
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Background
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Synonyms: Chromosome 21 open reading frame 70, CU070_HUMAN, Hypothetical protein LOC85395, PRED56, Uncharacterized protein C21orf70.
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 C21orf70 gene product has been provisionally designated C21orf70 pending further characterization.
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Gene ID
- 85395
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UniProt
- Q9NSI2
Target
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