C7orf34 Polyklonale Antilichaam, AbBy FluorTM 555 Vervoeging

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.

C7orf34; CG034_HUMAN; Chromosome 7 open reading frame 34; CTM 1; MSSP-binding protein CTM-1; Uncharacterized protein C7orf34.

135927

Cell membrane, Extracellular matrix

1-80/122

C7orf34

AbBy Fluor™ 555

KLH conjugated synthetic peptide derived from human C7orf34

WB, IF (IHC-P), IF (IHC-F), IF (ICC)

Purified by Protein A.

553nm/568nm

1µg/µl

WB (1:300-5000), IF (IHC-P) (1:50-200), IF (IHC-F) (1:50-200), IF (ICC) (1:50-200)

Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Unmodified

Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

135927

Human