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

Details for Product No. ABIN4998653
Target
Reactivity
Human, Mouse, Rat
23
17
16
2
2
2
2
1
1
1
1
1
Host
Rabbit
18
5
Clonality
Polyclonal
Conjugate
Alexa Fluor 680
1
1
1
1
1
1
1
1
1
1
1
1
1
Application
Immunofluorescence (Paraffin-embedded Sections) (IF (p))
12
9
5
3
1
Options
Immunogen KLH conjugated synthetic peptide derived from human C7orf10
Isotype IgG
Purification Purified by Protein A.
Target
Alternative Name C7orf10 (C7orf10 Antibody Abstract)
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
Application Notes IF(IHC-P) 1:50-200
Restrictions For Research Use only
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