Chromosome 7 Open Reading Frame 10 (C7orf10) antibody (Biotin) Primary Antibody
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- Target
- Chromosome 7 Open Reading Frame 10 (C7orf10)
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Clonality
- Polyclonal
- Conjugate
- Biotin
- Application
- Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C7orf10
- Isotype
- IgG
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- Application Notes
- WB 1:100-1000
IHC-P 1:100-500 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % sodium azide.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- 4 °C
- Storage Comment
- Store at 4°C
- Expiry Date
- 12 months
-
- Target
- Chromosome 7 Open Reading Frame 10 (C7orf10)
- Alternative Name
- C7orf10 (C7orf10 Antibody Abstract)
- Synonyms
- DERP13, ORF19, c7orf10, sugct, succinyl-CoA:glutarate-CoA transferase, succinyl-CoA:glutarate-CoA transferase L homeolog, SUGCT, sugct.L
- 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 C7orf10 gene product has been provisionally designated C7orf10 pending further characterization.
Synonyms: Chromosome 7 open reading frame 10, Dermal papilla derived protein 13, DERP13, FLJ11808, Hypothetical protein LOC79783, ORF19, Russel-Silver syndrome candidate, Uncharacterized protein C7orf10,CG010_HUMAN.
- Gene ID
- 79783