Transferrin Mouse Monoclonal Antibody [Clone ID: PTF-02]
CAT#: SM3156P
Transferrin mouse monoclonal antibody, clone PTF-02, Purified
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CNY 3140.00
货期*
                        5周
                    规格
                        | Cited in 1 publication. | 
Specifications
| Product Data | |
| Clone Name | PTF-02 | 
| Applications | ELISA, WB | 
| Recommend Dilution | ELISA. Western blot.  | 
        
| Reactivity | Porcine | 
| Host | Mouse | 
| Clonality | Monoclonal | 
| Specificity | The antibody PTF-02 recognizes porcine serum transferrin, a 77 kDa single polypeptide chain glycoprotein which is synthesised in the liver and consists of two domains each having a high affinity reversible binding site for Fe3+. The antibody is negative with Sheep and Horse. Other species not tested.  | 
        
| Isotype | IgG1 | 
| Formulation | Phosphate buffered saline (PBS) with 15 mM sodium azide, approx. pH 7.4 State: Purified State: Liquid Ig fraction  | 
        
| Concentration | lot specific | 
| Purification | Protein-A affinity chromatography; purity > 95% (by SDS-PAGE) | 
| Conjugation | Unconjugated | 
| Storage Condition | Store the antibody at 2 - 8 °C up to one month or (in aliquots) at -20 °C for longer. Avoid repeated freezing and thawing.  | 
        
| Database Link | |
| Background | Transferrin is a single polypeptide chain glycoprotein belonging to iron binding family of proteins. It has a molecular weight of 81,5 kDa (porcine). It is synthesised in the liver and consists of two domains each having a high affinity reversible binding site for Fe3+. The iron is transported in blood and interstitial fluids to sites of use and disposal. Iron/transferrin is essential in haemoglobin synthesis and for certain types of cell division. Serum concentration rises in iron deficiency and pregnancy and falls in iron overload, infection and inflammatory conditions. | 
| Synonyms | Serotransferrin, Siderophilin | 
| Reference Data | |
Citations (1)
| The use of this Antibodies has been cited in the following citations: | 
|---|
| 
                                                Dysfunction of the Voltage‐Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome
                                                ,null,
                                                Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
                                                ,PubMed ID 27287695
                                                [TF]
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