C7orf34 Polyclonal Antibody, PE-Cy5 Conjugated
Product Specifications
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 C7orf34 gene product has been provisionally designated C7orf34 pending further characterization.
Synonyms
C7orf34; CG034_HUMAN; Chromosome 7 open reading frame 34; CTM 1; MSSP-binding protein CTM-1; Uncharacterized protein C7orf34.
Gene ID
135927
Cellular Locus
Cell membrane, Extracellular matrix
Host
Rabbit
Immunogen
1-80/122
Target
C7orf34
Clonality
Polyclonal
Isotype
IgG
Conjugation
PE-Cy5
Source
KLH conjugated synthetic peptide derived from human C7orf34
Applications
WB
Purification
Purified by Protein A.
Excitation Emission
488nm/670nm
Concentration
1µg/µl
Dilution
WB (1:300-5000)
Buffer
Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Modification
Unmodified
Storage Conditions
Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
Product Datasheet
https://www.biossantibodies.com/datasheets/bs-15264R-PE-Cy5
Gene ID URL
135927
Predicted Cross Reactivity
Human
Curated Selection
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