ApoF(Center) polyclonal, anti-human antibody
€275.00
In stock
SKU
AC-ABV11272-100
Catalog Number: AC-ABV11272-100
Size: 100 µl
Host: Rabbit IgG
Applications: WB, IHC
Datasheet
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Size: 100 µl
Host: Rabbit IgG
Applications: WB, IHC
Datasheet
Request Information
Background:
Apolipoproteins are a family of fatty-acid binding proteins that transport fat through the bloodstream in the form of lipoproteins. ApoF (apolipoprotein F), also known as LTIP (lipid transfer inhibitor protein), is a 308 amino acid secreted protein that belongs to the apolipoprotein family. Expressed in liver tissues and also existing in plasma, ApoF inhibits the activity of CETP (cholesteryl ester transfer protein) and, via this inhibition, functions to regulate cholesterol transport. The gene encoding ApoF maps to human chromosome 12, which encodes over 1, 100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
Other Names:
APOF, Apolipoprotein F, Lipid transfer inhibitor protein
Primary Accession: Q13790
Gene Name: APOF
Gene ID: 319
Apolipoproteins are a family of fatty-acid binding proteins that transport fat through the bloodstream in the form of lipoproteins. ApoF (apolipoprotein F), also known as LTIP (lipid transfer inhibitor protein), is a 308 amino acid secreted protein that belongs to the apolipoprotein family. Expressed in liver tissues and also existing in plasma, ApoF inhibits the activity of CETP (cholesteryl ester transfer protein) and, via this inhibition, functions to regulate cholesterol transport. The gene encoding ApoF maps to human chromosome 12, which encodes over 1, 100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
Other Names:
APOF, Apolipoprotein F, Lipid transfer inhibitor protein
Primary Accession: Q13790
Gene Name: APOF
Gene ID: 319
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