Chromosome 7 Open Reading Frame 10 (C7orf10) antibody (Alexa Fluor 680)

Catalog No. ABIN4998653

Product Details

Target: Chromosome 7 Open Reading Frame 10 (C7orf10)

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Reactivity: Human, Mouse, Rat

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• Human 23
• Mouse 17
• Rat 16
• Cow 2
• Guinea Pig 2
• Horse 2
• Rabbit 2
• Bat 1
• Dog 1
• Monkey 1
• Pig 1
• Zebrafish (Danio rerio) 1

Host: Rabbit

Clonality: Polyclonal

Conjugate: Alexa Fluor 680

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• Un-conjugated 10
• Alexa Fluor 350 1
• Alexa Fluor 488 1
• Alexa Fluor 555 1
• Alexa Fluor 594 1
• Alexa Fluor 647 1
• Alexa Fluor 750 1
• Biotin 1
• Cy3 1
• Cy5 1
• Cy5.5 1
• Cy7 1
• FITC 1
• HRP 1

Application: Immunofluorescence (Paraffin-embedded Sections) (IF (p))

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• Immunofluorescence (Paraffin-embedded Sections) (IF (p)) 12
• Western Blotting (WB) 9
• ELISA 5
• Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)) 3
• Immunohistochemistry (IHC) 1

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf10

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % sodium azide.

Storage: 4 °C

Storage Comment: Store at 4°C

Expiry Date: 12 months

Target Details

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