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Thermo Fisher Scientific HBG1 Monoclonal Antibody (1G8)
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Thermo Fisher Scientific HBG1 Monoclonal Antibody (1G8)

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인간 HBG1 단백질을 인식하는 마우스 단클론 항체로 ELISA에 적합합니다. 친화 크로마토그래피로 정제되었으며 보존제가 없는 PBS 용액 형태입니다. 연구용으로만 사용되며 -20°C에서 보관합니다.

카탈로그번호
H00003047-M03
판매단위
pk
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마지막 업데이트 2025. 08. 03. 오전 12:34
Thermo Fisher Scientific H00003047-M03 HBG1 Monoclonal Antibody (1G8) 100 ug pk판매 단위 pk ·
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498,600원VAT 포함 548,460원

Thermo Fisher Scientific · Thermo Fisher Scientific HBG1 Monoclonal Antibody (1G8)

Applications

  • ELISA (ELISA)
    Tested Dilution: 3 ng/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2a, kappa
Class Monoclonal
Type Antibody
Clone 1G8
Immunogen HBG1 (AAH10913, 1–147 a.a) full-length recombinant protein with GST tag (GST tag MW: 26 kDa)
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage buffer PBS, pH 7.4
Contains No preservative
Storage conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Sequence of this protein is as follows:
MGHFTEEDKA TITSLWGKVN VEDAGGETLG RLLVVYPWTQ RFFDSFGNLS SASAVMGNPK VKAHGKKVLT SLGDAIKHLD DLKGTFAQLS ELHCDKLHVD PENFKLLGNV LVTVLAIHFG KEFTPEVQAS WQKMVTGVAS ALSSRYH

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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