Fetal Hemoglobin Test Kit, FITC
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Fetal Hemoglobin Test Kit, FITC

The Fetal Hemoglobin (HbF) Test is based on a monoclonal antibody directed to fetal hemoglobin (hemoglobin F). This antibody is자세히 알아보기
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HFH01100 Tests
카탈로그 번호 HFH01
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947,000
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Ends: 31-Mar-2026
1,114,000
할인액 167,000 (15%)
Each
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수량:
100 Tests
제품 가격(KRW)
947,000
Exklusiv online
Ends: 31-Mar-2026
1,114,000
할인액 167,000 (15%)
Each
카트에 추가하기
The Fetal Hemoglobin (HbF) Test is based on a monoclonal antibody directed to fetal hemoglobin (hemoglobin F). This antibody is conjugated with fluorescein (FITC). Commonly used, the fluorescein conjugates provide relatively high absorptivity, excellent fluorescence quantum yield, and good water solubility.

This reagent is intended for the identification followed by enumeration of fetal red blood cells. Fetal cells are identified by the presence of fetal hemoglobin using a flow cytometric method. The Fetal Hemoglobin Test may be used as an aid in identifying fetal-maternal hemorrhage and determining the need for immunoprophylaxis with immune globulin.

Antibody Specifications

Description:

Fetal Hemoglobin F (HbF), mouse IgG1 monoclonal

Label:

Fluorescein (FITC)

Validated Application:

Flow Cytometry

Species Reactivity:

Human

Ex/Em and laser configuration:

488/519 nm, blue laser

Clone ID:

HbF-1

Regulatory Status:

IVD

Antibody characteristics include:
• Clinical relevance
in vitro diagonstic


Clinical Relevance
The Fetal Hemoglobin Test contains a monoclonal antibody directed to HbF that specifically recognizes fetal hemoglobin found in fetal erythrocytes. The test permits the enumeration of fetal erythrocytes in the maternal circulation as a result of a fetal-maternal hemorrhage, or leakage, of fetal cells into the maternal circulation. 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. These conditions include hereditary anemic diseases such as sickle cell anemia and thalassemia major.

In Vitro Diagnostic
For In Vitro Diagnostic Use.

Related Links
Use the Spectraviewer to help you plan your experiments. Additional general information about Life Technologies flow cytometry products and support is also available.
For Research Use Only. Not for use in diagnostic procedures.
사양
항체 콘주게이트Classic Dyes (e.g. FITC, TRITC), FITC (Fluorescein)
검출 방법Fluorescence
용도(애플리케이션)Flow Cytometry Antibodies and Secondary Detection
형식Kit
라벨 또는 염료FITC (Fluorescein)
수량100 Tests
배송 조건Wet Ice
Mouse
유형Hemoglobin Test Kit
CE 마커Yes
Unit SizeEach
구성 및 보관
Store in refrigerator (2°C to 8°C).

인용 및 참조 문헌 (6)

인용 및 참조 문헌
Abstract
Detection of fetomaternal hemorrhage.
Authors:Kim YA, Makar RS,
Journal:Am J Hematol
PubMed ID:22231030
'The prevention of Rhesus D alloimmunization through Rh immune globulin (RhIg) administration is the major indication for the accurate detection and quantification of fetomaternal hemorrhage (FMH). In the setting of D incompatibility, D-positive fetal cells can sensitize the D-negative mother, resulting in maternal anti-D alloantibody production. These anti-D alloantibodies may ... More
Site-specific gene correction of a point mutation in human iPS cells derived from an adult patient with sickle cell disease.
Authors:Zou J, Mali P, Huang X, Dowey SN, Cheng L,
Journal:Blood
PubMed ID:21881051
'Human induced pluripotent stem cells (iPSCs) bearing monogenic mutations have great potential for modeling disease phenotypes, screening candidate drugs, and cell replacement therapy provided the underlying disease-causing mutation can be corrected. Here, we report a homologous recombination-based approach to precisely correct the sickle cell disease (SCD) mutation in patient-derived iPSCs ... More
Estimation of
Authors:Roys JL, Warzynski MJ,
Journal:Cytometry B Clin Cytom
PubMed ID:16059876
Improving laboratory practice: looking at fetal hemoglobin histograms.
Authors:Warzynski MJ, Roys JL,
Journal:Cytometry B Clin Cytom
PubMed ID:14994377
Tracking donor RBC survival in premature infants: agreement of multiple populations of biotin-labeled RBCs with Kidd antigen-mismatched RBCs.
Authors:Widness JA, Nalbant D, Matthews NI, Strauss RG, Schmidt RL, Cress GA, Zimmerman MB, Mock DM,
Journal:
PubMed ID:24108188
Anemia, a common condition among critically ill premature infants, is affected by red blood cell (RBC) survival (RCS). We hypothesized that transfused allogeneic Kidd antigen-mismatched RBCs would demonstrate the same concurrent RCS tracking as RBCs multilabeled at separate, discrete low densities with biotin (BioRBCs). Allogeneic RBCs from adult donors were ... More