C7orf64 antibody (AA 1-100) (AbBy Fluor® 680)
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- Target See all C7orf64 Antibodies
- C7orf64 (Chromosome 7 Open Reading Frame 64 (C7orf64))
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Binding Specificity
- AA 1-100
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C7orf64 antibody is conjugated to AbBy Fluor® 680
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Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Human
- Predicted Reactivity
- Mouse,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C7orf64
- Isotype
- IgG
- Top Product
- Discover our top product C7orf64 Primary Antibody
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- Application Notes
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- C7orf64 (Chromosome 7 Open Reading Frame 64 (C7orf64))
- Alternative Name
- C7orf64 (C7orf64 Products)
- Synonyms
- C7orf64 antibody, DKFZP564O0523 antibody, HSPC304 antibody, RGD1310794 antibody, AW548102 antibody, C030048B08Rik antibody, dkfzp564o0523 antibody, C4H7orf64 antibody, RNA binding motif protein 48 antibody, rbm48 antibody, RBM48 antibody, Rbm48 antibody
- Background
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Synonyms: C7orf64, RBM48_HUMAN, DKFZP564O0523, DKFZp686D1651, HSPC304, Hypothetical protein LOC84060, OTTHUMP00000215752, UPF0712 protein C7orf64.
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 C7orf64 gene product has been provisionally designated C7orf64 pending further characterization.
- Gene ID
- 84060
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