
Thermo Fisher Scientific Hemoglobin beta F Monoclonal Antibody (4B3.B5.F3.B7)
인간 HbF 감마 이소폼에 특이적으로 반응하는 단클론 항체로, Western blot, ELISA, Immunoprecipitation에 사용 가능. 마우스 IgG1, kappa 형식의 비결합 항체이며, -20°C에서 보관. 연구용으로만 사용 가능.
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Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1 µg/mL |
| ELISA | 1:20,000 |
| Immunoprecipitation (IP) | 1 µg/mL |
Product Specifications
| 항목 | 내용 |
|---|---|
| Host / Isotype | Mouse / IgG1, kappa |
| Class | Monoclonal |
| Type | Antibody |
| Clone | 4B3.B5.F3.B7 |
| Immunogen | Anti-Hemoglobin beta F Monoclonal Antibody was produced in mice by repeated immunizations with a synthetic peptide corresponding to amino acid residues near the N-terminus of Hb beta-subunit conjugated to KLH. |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Storage conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
Store vial at -20°C prior to opening.
This product is stable at 4°C as an undiluted liquid.
For extended storage, aliquot contents and freeze at -20°C or below.
Avoid cycles of freezing and thawing.
Dilute only prior to immediate use.
Reacts specifically with human HbF gamma isoform.
This antibody does not react with the HbA, HbS, HbC, or HbA-2 isoforms.
Target Information
Hemorrhage of cells from an Rh+ fetus into the circulation of an Rh- mother may result in the formation of Rh-reactive antibodies in the mother. Rh hemolytic anemia in a subsequent Rh+ fetus may result from placental transfer of antibodies formed in the mother to the fetus.
Although the volume of fetal erythrocytes found in the maternal circulation during pregnancy and immediately post-partum is reported to be small and of uncertain clinical significance in many cases, substantial hemorrhage may result from a number of causes including fetal or maternal trauma and placental defects.
Erythrocytes containing fetal hemoglobin may be found in individuals of any age, but with lower amounts of fetal hemoglobin compared to fetal red cells. These cells have been termed F cells.
High levels of F cells may also exist in adults with a heterogeneous group of genetic disorders of uncertain etiology, referred to as Hereditary Persistence of Fetal Hemoglobin.
Other clinical conditions causing significant levels of anemia may also result in elevated levels of F cells. Several clinical conditions have been described with increased levels of F cells, including hereditary anemic diseases such as sickle cell anemia and thalassemia major.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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