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Invitrogen™ FAM221A Polyclonal Antibody
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Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA554065

Catalog No. PIPA554065


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Description

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.
TRUSTED_SUSTAINABILITY
Specifications

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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