SKU: WP5805 Categories: ,

TF Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP5805-100
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Product details

Background:

transferrin(TF) Homo sapiens This gene encodes a glycoprotein with an approximate molecular weight of 76.5 kDa. It is thought to have been created as a result of an ancient gene duplication event that led to generation of homologous C and N-terminal domains each of which binds one ion of ferric iron. The function of this protein is to transport iron from the intestine, reticuloendothelial system, and liver parenchymal cells to all proliferating cells in the body. This protein may also have a physiologic role as granulocyte/pollen-binding protein (GPBP) involved in the removal of certain organic matter and allergens from serum. [provided by RefSeq, Sep 2009],

Specifications

Size50μL/100μL
TargetTransferrin
ReactivityHuman, Mouse, Rat
ApplicationsWB, IHC, IF
MW(Calculated)
MW(Observed)77kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-10000; IHC 1:200-500; IF 1:50-200 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationPBS, pH 7.4, containing 0.5%BSA, 0.02% sodium azide as Preservative and 50% Glycerol.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from part region of human protein AA range: 230-310
SpecificityThe antibody detects endogenous TF protein.
Gene NameTF
Protein NameSerotransferrin
Other NameTF; / Serotransferrin; / Transferrin; / Beta-1 metal-binding globulin; / Siderophilin
SpeciesHuman
Gene ID7018
UniprotP02787,
Species.1Mouse
Gene ID.122041
Uniprot.1Q921I1,
Species.2Rat
Gene ID.224825
Uniprot.2P12346
Cellular LocalizationSecreted.
Tissue ExpressionExpressed by the liver and secreted in plasma.
Signaling_pathwayCellular Processes >> Cell growth and death >> Ferroptosis;Environmental Information Processing >> Signal transduction >> TGF-beta signaling pathway;Environmental Information Processing >> Signal transduction >> HIF-1 signaling pathway
Research Areas>>HIF-1 signaling pathway; / >>Ferroptosis; / >>Mineral absorption
FunctionDisease:Defects in TF are the cause of atransferrinemia [MIM:209300]. Atransferrinemia is rare autosomal recessive disorder characterized by iron overload and hypochromic anemia.,Function:Transferrins are iron binding transport proteins which can bind two Fe(3+) ions in association with the binding of an anion, usually bicarbonate. It is responsible for the transport of iron from sites of absorption and heme degradation to those of storage and utilization. Serum transferrin may also have a further role in stimulating cell proliferation.,online information:Transferrin entry,polymorphism:Different polymorphic variants of transferrin are known. The sequence shown is the predominant electrophoretic variant (C1 or TF*C1).,similarity:Belongs to the transferrin family.,similarity:Contains 2 transferrin-like domains.,subunit:Monomer.,tissue specificity:Expressed by the liver and secreted in plasma.,
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