CD105 (ENG) Rabbit Polyclonal Antibody

CAT#: DP3517

CD105 (ENG) rabbit polyclonal antibody, Purified

Size: 100 ug 200 ug


USD 355.00

2 Weeks*

Size
    • 200 ug

Specifications

Product Data
Applications ELISA, FC, IF, IHC, WB
Recommended 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).
Reactivities 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 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.
Stability Shelf life: one year from despatch.
Gene Name endoglin
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
Reference Data

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*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.