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Invitrogen™ FAM221A Polyclonal Antibody

Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA554065
Description
Immunogen sequence: SGFHSCFTCA CGQPAYAHDT VVETKQERLA QEKPVGQDIP YAAMGGLTGF SSLAEGYMRL DDSGIGVP Highest antigen sequence identity to the following orthologs: Mouse - 91%, Rat - 94%.
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.
Specifications
FAM221A | |
Polyclonal | |
Unconjugated | |
FAM221A | |
C7orf46; FAM221A; family with sequence similarity 221 member A; family with sequence similarity 221, member A; protein FAM221A; uncharacterized protein C7orf46 | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
340277 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Immunohistochemistry (Paraffin) | |
0.3 mg/mL | |
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2 | |
A4D161 | |
FAM221A | |
Recombinant protein corresponding to Human FAM221A. Recombinant protein control fragment (Product #RP-92836). | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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