CD133 Protein - ACROBiosystems

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CD133

Brief Information

Name:CD133
Target Synonym:Antigen AC133,Prominin-1,PROM1,Prominin 1,Prominin-Like Protein 1,PROML1,Stargardt Disease 4 (Autosomal Dominant),Hematopoietic Stem Cell Antigen,Macular Dystrophy, Retinal 2,Prominin (Mouse)-Like 1,CD133 Antigen,HProminin,MSTP061,CORD12,AC133,CD133,MCDR2

Number of Launched Drugs:0
Number of Drugs in Clinical Trials:0
Lastest Research Phase:Preclinical


CD3-H52H1	Human	Human CD133 Full Length Protein, His Tag (Nanodisc)
CD3-H82E6	Human	Biotinylated Human CD133 Protein, His,Avitag™ (Nanodisc)
CD3-H52H4	Human	Human CD133 Protein, His Tag

Cat. No.

Species

Product Description

Structure

Purity

Feature

CD3-H52H1

Human

Human CD133 Full Length Protein, His Tag (Nanodisc)

CD3-H82E6

Human

Biotinylated Human CD133 Protein, His,Avitag™ (Nanodisc)

CD3-H52H4

Human

Human CD133 Protein, His Tag

Part of Bioactivity data

CD3-H52H4-ELISA

Immobilized Human CD133, His Tag (Cat. No. CD3-H52H4) at 1 μg/mL (100 μL/well) can bind Monoclonal Anti-Human CD133 (133-3) Antibody, Human IgG1 with a linear range of 1-16 ng/mL (QC tested).

Protocol

CD3-H52H1-ELISA

Immobilized Human CD133 Full Length, His Tag (Nanodisc) (Cat. No. CD3-H52H1) at 1 μg/mL (100 μL/well) can bind Monoclonal Anti-Human CD133 (133-3) Antibody, Human IgG1 with a linear range of 0.2-4 ng/mL (QC tested).

Protocol

Synonym Name

CD133,PROM1,PROML1,Prominin-1,AC133

Background

Prominin-1 is also known as CD133, Antigen AC133, PROM1, PROML1 and MSTP061. Is used as marker for hematopoietic stem and progenitor cells (HSPC) for somatic stem cell isolation. May play a role in cell differentiation, proliferation and apoptosis . Binds cholesterol in cholesterol-containing plasma membrane microdomains and may play a role in the organization of the apical plasma membrane in epithelial cells. During early retinal development acts as a key regulator of disk morphogenesis. Involved in regulation of MAPK and Akt signaling pathways. In neuroblastoma cells suppresses cell differentiation such as neurite outgrowth in a RET-dependent manner.

Clinical and Translational Updates