C7ORF57 antibody (AA 161-260) (Biotin)
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- Target See all C7ORF57 products
- C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))
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Binding Specificity
- AA 161-260
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Reactivity
- Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C7ORF57 antibody is conjugated to Biotin
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Application
- Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA
- Cross-Reactivity
- Rat
- Predicted Reactivity
- Human,Mouse,Cow,Sheep,Horse
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C7orf57
- Isotype
- IgG
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- Application Notes
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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
- C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))
- Alternative Name
- C7orf57 (C7ORF57 Products)
- Synonyms
- C7orf57 antibody, chromosome 4 open reading frame, human C7orf57 antibody, chromosome 7 open reading frame 57 antibody, C4H7orf57 antibody, C7orf57 antibody
- Background
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Synonyms: C7orf57, CG057_HUMAN, Chromosome 7 open reading frame 57, Uncharacterized protein C7orf57.
Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf57 gene product has been provisionally designated C7orf57 pending further characterization.
- Gene ID
- 136288
- UniProt
- Q8NEG2
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