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Moyamoya Disease: Disease Bioinformatics

Research of Moyamoya Disease has been linked to Arterial Occlusive Diseases, Hemorrhage, Cerebrovascular Accident, Stenosis, Cerebrovascular Disorders. The study of Moyamoya Disease has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Moyamoya Disease include Pathogenesis, Angiogenesis, Coagulation, Localization, Transposition. These pathways complement our catalog of research reagents for the study of Moyamoya Disease including antibodies and ELISA kits against ICA, MMD, EMD, MCA, FLVCR1.

Moyamoya Disease Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Moyamoya Disease below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 961 products for the study of Moyamoya Disease that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP2-55515
Immunocytochemistry/Immunofluorescence: MMD Antibody [NBP2-55515] - Staining of human cell line U-2 OS shows localization to vesicles.

Rabbit Polyclonal
Species Human
Applications ICC/IF

NBP1-87692
Western Blot: Emerin Antibody [NBP1-87692] - Analysis in RT-4 cells transfected with control siRNA, target specific siRNA probe #1 and #2. Remaining relative intensity is presented. Loading control: Anti-GAPDH.Immunocytochemistry/Immunofluorescence: Emerin Antibody [NBP1-87692] - Staining of human cell line U-251 MG shows localization to nuclear membrane & endoplasmic reticulum. Antibody staining is shown in green.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, ICC/IF, IHC

5 Publications
NBP2-14019
Immunocytochemistry/Immunofluorescence: FLVCR Antibody [NBP2-14019] - Immunofluorescent staining of human cell line CACO-2 shows localization to cell junctions.Immunohistochemistry-Paraffin: FLVCR Antibody [NBP2-14019] - Staining of human small intestine shows strong membranous positivity in glandular cells.

Rabbit Polyclonal
Species Human
Applications ICC/IF, IHC, IHC-P

7954-GM/CF


Species Human

1 Publication
NBP2-42388
Immunohistochemistry-Paraffin: LAMC2 Antibody (CL2980) [NBP2-42388] - Staining in human fallopian tube and liver tissues. Corresponding LAMC2 RNA-seq data are presented for the same tissues.Western Blot: LAMC2 Antibody (CL2980) [NBP2-42388] - Analysis in A-431 cells transfected with control siRNA, target specific siRNA probe #1 and #2, using Anti-LAMC2 antibody. Remaining relative intensity is presented. Loading control: Anti-GAPDH.

Mouse Monoclonal
Species Human
Applications WB, ICC/IF, IHC

2 Publications
233-FB/CF
Recombinant Human FGF basic/FGF2/bFGF (146 aa) (Catalog # 233-FB/CF) stimulates cell proliferation of the NR6R‑3T3 mouse fibroblast cell line. The activity is approximately 3-fold greater than the top competitor's FGF basic (146 aa).1 µg/lane of Recombinant Human FGF basic/FGF2/bFGF (146 aa) was resolved by SDS-PAGE with silver staining, under reducing (R) conditions, showing a band at 17 kDa.


Species Human

398 Publications
DVE00
 VEGF [HRP] VEGF [HRP]


Species Human

     26 Reviews

541 Publications
H00005555-P01
SDS-Page: Recombinant Human PRH2 Protein [H00005555-P01] - 12.5% SDS-PAGE Stained with Coomassie Blue.


Species Human

NBP1-76289
Western Blot: NLRP5 Antibody [NBP1-76289] - Mouse brain tissue lysate with NLRP5 antibody at 1 ug/mL in (A) the absence and (B) the presence of blocking peptide.Immunocytochemistry/Immunofluorescence: NLRP5 Antibody [NBP1-76289] - Immunofluorescence of NALP5 in human brain tissue with NALP5 antibody at 20 ug/mL.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, ELISA, ICC/IF

NBP1-91705
Western Blot: BRAP Antibody [NBP1-91705] - Lane 1: NIH-3T3 cell lysate (Mouse embryonic fibroblast cells). Lane 2: NBT-II cell lysate (Rat Wistar bladder tumor cells).Immunocytochemistry/Immunofluorescence: BRAP Antibody [NBP1-91705] - Immunofluorescent staining of human cell line U-2 OS shows localization to nuclear membrane & cytosol.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, ICC/IF, IHC

MAB98901
    Western  blot shows lysates of Jurkat human acute T cell leukemia cell line,  NIH‑3T3 mouse embryonic fibroblast cell line, and C6 rat glioma  cell line. PVDF membrane was probed with 1 µg/mL of Mouse Anti-Human/Mouse/Rat  IMPA1/IMP1 Monoclonal Antibody (Catalog # MAB98901) followed by  HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # <a class=

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB

NB300-155
Western Blot: Neurofibromin 1 Antibody [NB300-155] - Western Blot of (A, B, C above).Immunohistochemistry: Neurofibromin 1 Antibody [NB300-155] - NF1 protein labeling displays positive signal in the maturing and the hypertrophic cartilages but only faint labeling in the proliferative cartilage.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, ICC/IF, IHC

4 Publications
DADT130
 ADAMTS13 [HRP] ADAMTS13 [HRP]


Species Human

     1 Review

8 Publications
NBP1-88466
Western Blot: RNF213 Antibody [NBP1-88466] - Analysis in human cell lines A-549 and HEK293 using anti-RNF213 antibody. Corresponding RNF213 RNA-seq data are presented for the same cell lines. Loading control: anti-HDAC1.Western Blot: RNF213 Antibody [NBP1-88466] - TRAIP activity is required for Mcm7 ubiquitylation in mitosis. The same experiment from Fig 3B but with addition of the RNF213 blot. An asterisk

Rabbit Polyclonal
Species Human, Xenopus
Applications WB, ICC/IF, IHC

2 Publications

Related PTMs

Moyamoya Disease has been studied in relation to posttranslational modifications (PTMs) including:

Alternate Names

Moyamoya Disease is also known as moyamoya disease, moyamoya disease 3, progressive intracranial arterial occlusion (disorder), spontaneous occlusion of the circle of willis, moyamoya disease, secondary, moyamoya disease (disorder), moyamoya disease, primary, moyamoya disease 1, moyamoya disease 2, moyamoya syndrome.