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MOUSE ANTI HUMAN CD44:FITC
MOUSE ANTI HUMAN CD44:FITC
- 中文名称：
- MOUSE ANTI HUMAN CD44:FITC
- 英文名称：
- MOUSE ANTI HUMAN CD44:FITC
- 品牌：
- AAA Biotech
- 品牌介绍：
- AAA Biotech专注于为全球生命科学研究提供高品质的蛋白质研究工具，核心产品包括经严格验证的抗体、重组蛋白及ELISA试剂盒。
- 货号：
- AAA50483
- 规格：
- 0.1 mg|2x0.1 mg|3x0.1 mg|4x0.1 mg|5x0.1 mg
- 保存建议：
- IgG concentration 0.1mg/ml
- 货期：
- 6-8周
- 来源宿主：
- Mouse
- 反应种属：
- Human, Cat, Baboon, African green monkey
- 应用：
- FCM/FACS (Flow Cytometry)
- 免责声明：
- *本产品仅供科研实验使用，不得用于临床诊断。*
- 其他：
克隆性:Monoclonal
同型:IgG2a
克隆号:[156-3C11]
特异性:N/A
纯度:Purified IgG prepared by affinity chromatography on Protein A from tissue culture supernatant
形式：Purified IgG conjugated to Fluorescein Isothiocyanate Isomer 1 (FITC) - liquid
ALEXA FLUOR 647, FITC, Purified, RPE
Phosphate buffered saline
0.09% Sodium Azide (NaN3)
1% Bovine Serum Albumin
浓度：IgG concentration 0.1mg/ml
- 说明书：
Mouse anti Human CD44 antibody, clone 156-3C11 recognizes human Phagocytic glycoprotein 1 also known as CD44, HCAM or CD44s. CD44 is a ~90 kDa single pass type I transmembrane glycoprotein. Various isoforms of CD44 exist due to differential expression of exon products form the membrane proximal region of the extracellular domain. Mouse anti Human CD44 antibody, clone 156-3C11 recognizes the ~90 kDa standard form lacking any of the alternative spliced products, the clone is expected to recognize all isoforms of CD44. CD44 is expressed on leucocytes, erythrocytes, white matter of the brain and some epithelial cells of the breast and small intestine. Antibodies produced by clone 156-3C11 recognise epitope 3, defined as a protease resistant epitope on the CD44 molecule (CD44 and CD45R Cluster report. In Leucocyte Typing V. White cell differentiation antigens. Eds Schlossman, S.F. et al). CD44 is a receptor for hyaluronic acid (HA) and is involved in cell-cell interactions, cell adhesion and migration (Lesley et al. 1990). CD44 also participates in a wide variety of cellular functions including lymphocyte activation, recirculation and homing (Shimizu et al. 1989). CD44 expression may be up-regulated upon some carcinomas, and it has been speculated that this may be related to metastatic potential (East and Hart 1993).
