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M-CSF / CSF-1 항체, 토끼 다클론 항체, Antigen Affinity Purified

데이터시트리뷰프로토콜
발현 숙주: Yeast  
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11792-H08Y-20
11792-H08Y-10
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발현 숙주: Human Cells  
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11792-HNAH-20
11792-HNAH-10
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10 µg 
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제품 설명: Active  
발현 숙주: Human Cells  
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11792-H08H-5
11792-H08H-20
11792-H08H-100
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발현 숙주: Human Cells  
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11792-H02H-50
11792-H02H-5
11792-H02H-100
11792-H02H-10
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발현 숙주: Human Cells  
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11792-H08H1-20
11792-H08H1-10
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발현 숙주: Human Cells  
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51112-M08H-5
51112-M08H-20
51112-M08H-100
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발현 숙주: Human Cells  
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51112-MNAH-5
51112-MNAH-20
51112-MNAH-100
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발현 숙주: Human Cells  
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90029-C08H-50
90029-C08H-10
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발현 숙주: Human Cells  
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90029-C02H-50
90029-C02H-10
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10 µg 
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M-CSF/CSF-1 antibody 연구배경

Macrophage colony-stimulating factor 1, also known as CSF-1, M-CSF, Lanimostim and CSF1, is a single-pass membrane protein which is disulfide-linked as a homodimer or heterodimer. Granulocyte / macrophage colony-stimulating factors are cytokines that act in hematopoiesis by controlling the production, differentiation, and function of 2 related white cell populations of the blood, the granulocytes and the monocytes-macrophages. M-CSF/CSF-1 is known to facilitate monocyte survival, monocyte-to-macrophage conversion, and macrophage proliferation. M-CSF/CSF-1 is a secreted cytokine which influences hemopoietic stem cells to differentiate into macrophages or other related cell types. It binds to the Colony stimulating factor 1 receptor. M-CSF/CSF-1 may also be involved in development of the placenta. The active form of M-CSF/CSF-1 is found extracellularly as a disulfide-linked homodimer, and is thought to be produced by proteolytic cleavage of membrane-bound precursors. M-CSF/CSF-1 induces cells of the monocyte/macrophage lineage. It also plays a role in immunological defenses, bone metabolism, lipoproteins clearance, fertility and pregnancy. Upregulation of M-CSF/CSF-1 in the infarcted myocardium may have an active role in healing not only through its effects on cells of monocyte/macrophage lineage, but also by regulating endothelial cell chemokine expression.

 M-CSF/CSF-1 antibody 참고자료
  1. Pandit J. et al., 1992, Science. 258: 1358-62.
  2. Tokai M. et al., 2000, J Bacteriol. 182 (10): 2865-8.
  3. Fan X. et al., 2001, Am J Physiol Endocrinol Metab. 280 (1): E103-11.
  4. Frangogiannis NG. et al., 2003, Am J Physiol Heart Circ Physiol. 285 (2): H483-92.
  5. Cupp JS. et al., 2007, Am J Surg Pathol. 31 (6): 970-6.
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