CD105 (ENG) Rabbit Polyclonal Antibody
CAT#: DP3517
CD105 (ENG) rabbit polyclonal antibody, Purified
Size: 100 ug
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CNY 3,720.00
货期*
5周
规格
Specifications
Product Data | |
Applications | ELISA, FC, IF, IHC, WB |
Recommend Dilution | ELISA (1-15 µg/ml). Western blot (1-5 µg/ml with the appropriate secondary reagents). FACS analysis and cell sorting (2-5 µg/ml together with the appropriate secondary reagents). Immunofluorescence/Immunohistochemistry (1-5 µg/ml). |
Reactivity | Human |
Host | Rabbit |
Clonality | Polyclonal |
Immunogen | Recombinant Human soluble CD105/Endoglin (aa. 22 (Glu) to 586 (Leu)) derived from Insect Cells (Cat.-No DA3523X). |
Specificity | This antibody detects CD105. |
Formulation | PBS, pH 7.4 without preservatives State: Purified State: Lyophilized purified Ig fraction |
Reconstitution Method | Restore in sterile water to a concentration of 0.1-1.0 mg/ml |
Purification | Protein A Chromatography |
Conjugation | Unconjugated |
Storage Condition | Prior to reconstitution store at 2-8°C. Following reconstitution store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
Gene Name | endoglin |
Database Link | |
Background | Endoglin, also known as CD105, is a Type I integral membrane glycoprotein with a large, disulfide-linked, extracellular region and a short, constitutively phosphorylated, cytoplasmic tail. Two splice variants of human Endoglin, the S-Endoglin and L-Endoglin that differ in the length of their cytoplasmic tails have been identified. Endoglin is highly expressed on vascular endothelial cells, chondrocytes, and syncytiotrophoblasts of term placenta. It is also found on activated monocytes, bone marrow pro-erythroblasts, and leukemic cells of lymphoid and myeloid lineages. Human and mouse Endoglin share approximately 70% and 97 % amino acid sequence identity in their extracellular and intracellular domains, respectively. It has clearly been shown that CD105/Endoglin is required for angiogenesis and it plays a key role in heart development. Mutations in human Endoglin or ALK-1 (another type I serine/threonine receptor) lead to the vascular disorder hereditary hemorrhagic telangiectasia (HHT). Mice heterozygous for Endoglin have been developed as disease models for HHT. Endoglin has been shown to be a powerful marker of neovascularization. It is also useful as a functional marker that defines long-term repopulating hematopoietic stem cells. |
Synonyms | ENG, END, HHT1, ORW, ORW1 |
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