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Alagille Syndrome: Disease Bioinformatics

Research of Alagille Syndrome has been linked to Cholestasis, Liver Diseases, Intrahepatic Cholestasis, Biliary Atresia, Dysplasia. The study of Alagille Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Alagille Syndrome include Notch Signaling Pathway, Pathogenesis, Excretion, Localization, Liver Development. These pathways complement our catalog of research reagents for the study of Alagille Syndrome including antibodies and ELISA kits against NOTCH, GROWTH HORMONE, JAG1, APOA1, STS.

Top Research Reagents

We have 2096 products for the study of Alagille Syndrome that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.

Notch-1 Antibody (mN1A) - BSA Free
NB100-78486
Knockout Validated: Notch-1 Antibody (mN1A) [NB100-78486] - Lysates of HeLa human cervical epithelial carcinoma parental cell line and Notch-1 knockout (KO) HeLa cell line. PVDF membrane was probed with 2.0 ug/mL of Mouse Anti-Human Notch-1 Monoclonal Antibody (Catalog # NB100-78486) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog #HAF018). Specific band was detected for Notch-1 at approximately 110 kDa (as indicated) in the parental HeLa cell line, but is not detectable in the knockout HeLa cell line. This experiment was conducted under reducing conditions.Western Blot: Notch-1 Antibody (mN1A) [NB100-78486] - Cell extracts from Jurkat (Lane 1) or mouse thymocytes (Lane 2) were analyzed with monoclonal anti-NOTCH1 antibody. The mN1A antibody recognizes both mouse and human 270 kDa full-length NOTCH1 and 110-120 kDa cleaved NOTCH 1 (NICD).

Mouse Monoclonal
Species Human, Mouse, Rat (Negative)
Applications WB, Flow, ICC/IF

     2 Reviews

10 Publications
Notch-3 Antibody (1G5)
H00004854-M01
ELISA: Notch-3 Antibody (1G5) [H00004854-M01] - Detection limit for recombinant GST tagged NOTCH3 is approximately 0.03ng/ml as a capture antibody.

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

     1 Review

13 Publications
csl/RBPJK Antibody
NBP1-33427
Western Blot: csl/RBPJK Antibody [NBP1-33427] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with csl/RBPJK antibody [C1C3] (NBP1-33427) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody,Immunocytochemistry/Immunofluorescence: csl/RBPJK Antibody [NBP1-33427] - Analysis of paraformaldehyde-fixed HeLa at 1:100 dilution.

Rabbit Polyclonal
Species Human
Applications WB, ICC/IF, ChIP

     1 Review

1 Publication
HES-1 Antibody (OTI4H1)
NBP1-47791
Western Blot: HES-1 Antibody (OTI4H1) [NBP1-47791] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY HES1 (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-HES1 (1:500).Immunocytochemistry/Immunofluorescence: HES-1 Antibody (OTI4H1) [NBP1-47791] - HeLa cells using anti-HES1 mouse monoclonal antibody.

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

8 Publications
ABCB11 Antibody
NBP1-89319
Immunohistochemistry-Paraffin: ABCB11 Antibody [NBP1-89319] - Staining in human liver and skeletal muscle tissues . Corresponding ABCB11 RNA-seq data are presented for the same tissues.Immunohistochemistry: ABCB11 Antibody [NBP1-89319] - Histopathology of ABCB11 disease. (a) Giant-cell hepatitis (arrows) with hepatocanalicular cholestasis and (b) complete absence of ABCB11/BSEP protein are typical findings in PFIC2 patients. Inset: immunohistochemical positivity of BSEP in the apical (canalicular) domain of hepatocytes in a healthy control. (a) Hematoxylin and eosin, original magnification x200. (b, inset) Immunohistochemical staining with ABCB11 Rabbit Polyclonal Antibody (NBP1-89319, Novus Biologicals, USA), original magnification x200 (b), x400 (inset). Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/30148122) licensed under a CC-BY license.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

5 Publications
BRIC Antibody
NBP1-90068
Immunohistochemistry-Paraffin: BRIC Antibody [NBP1-90068] - Staining in human rectum and lymph node tissues using anti-ATP8B1 antibody. Corresponding ATP8B1 RNA-seq data are presented for the same tissues.Immunohistochemistry-Paraffin: BRIC Antibody [NBP1-90068] - Staining of human cerebral cortex, kidney, liver and lymph node using Anti-ATP8B1 antibody NBP1-90068 (A) shows similar protein distribution across tissues to independent antibody NBP1-90067 (B).

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

Steroid sulfatase Antibody
NBP1-90095
Immunohistochemistry-Paraffin: Steroid sulfatase Antibody [NBP1-90095] - Staining of human placenta shows high expression.Immunohistochemistry-Paraffin: Steroid sulfatase Antibody [NBP1-90095] - Staining of human pancreas shows low expression as expected.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

3 Publications
MDR3/ABCB4 Antibody
NBP2-30876
Immunohistochemistry-Paraffin: MDR3/ABCB4 Antibody [NBP2-30876] - Staining of human skeletal muscle shows no positivity in myocytes as exected.Immunohistochemistry-Paraffin: MDR3/ABCB4 Antibody [NBP2-30876] - Staining of human cerebral cortex shows no positivity in neurons as expected.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

1 Publication
Serpin A3N Antibody [Unconjugated]
AF4709

Goat Polyclonal
Species Mouse
Applications WB, IP

32 Publications
Notch-2 Antibody [Unconjugated]
AF3735
Notch‑2 was detected in immersion fixed paraffin-embedded sections of human kidney using Goat Anti-Human Notch‑2 Intracellular Domain Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3735) at 5 µg/ml for 1 hour at room temperature followed by incubation with the Anti-Goat IgG VisUCyte™ HRP Polymer Antibody (Catalog # <a class=NoLineLink href=

Goat Polyclonal
Species Human
Applications WB, IHC

6 Publications
Notch-4 Antibody [Unconjugated]
AF3847
Notch‑4 was detected in immersion fixed SH‑SY5Y human neuroblastoma cell line using Goat Anti-Human Notch‑4 Intracellular Domain Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3847) at 15 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Goat IgG Secondary Antibody (red; <a class=NoLineLink href=

Goat Polyclonal
Species Human
Applications WB, ICC

2 Publications
Jagged 1 [Unconjugated]
1277-JG


Species Human
Applications BA

45 Publications
BMP-2 [Unconjugated]
355-BM
Recombinant human/mouse/rat BMP-2 (<a class=NoLineLink href=


Species Human, Mouse, Rat
Applications BA

190 Publications
EGF [Unconjugated]
236-EG
Recombinant Human EGF Protein (Catalog # 236-EG) has a molecular weight (MW) of 6.7 kDa as analyzed by SEC-MALS, suggesting that this protein is a monomer.Recombinant Human EGF (Catalog # 236‑EG) stimulates cell proliferation of the Balb/3T3 mouse embryonic fibroblast cell line. The ED<sub>50</sub> for this effect is 20‑100 pg/mL.


Species Human
Applications BA

836 Publications
Cytokeratin 7 Antibody (OV-TL12/30) - Azide and BSA Free
NBP2-47940
Western Blot: Cytokeratin 7 Antibody (OV-TL12/30) - Azide and BSA Free [NBP2-47940] - Western Blot Analysis of human HeLa cell lysate using Cytokeratin 7 Antibody (OV-TL12/30).Immunocytochemistry/Immunofluorescence: Cytokeratin 7 Antibody (OV-TL12/30) - Azide and BSA Free [NBP2-47940] - Immunofluorescent staining of methanol-fixed HeLa cells. Cytokeratin 7 Antibody (OV-TL12/30) followed by goat anti-Mouse IgG-CF488 (Green). The nuclear counterstain is Red Dot.

Mouse Monoclonal
Species Human, Mouse
Applications WB, Simple Western, Flow

     1 Review

1 Publication
Apolipoprotein A-I/ApoA1 Antibody - BSA Free
NBP2-52979
Immunocytochemistry/Immunofluorescence: Apolipoprotein A-I/ApoA1 Antibody - BSA Free [NBP2-52979] - HepG2 cells were fixed in 4% paraformaldehyde for 10 minutes and permeabilized in 0.05% Triton X-100 in PBS for 5 minutes. The cells were incubated with Apolipoprotein A-1/ApoA1 Antibody (NBP2-52979) at 1ug/ml overnight at 4C and detected with an anti-rabbit DyLight 488 (Green) at a 1:1000 dilution for 60 minutes. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.Western Blot: Apolipoprotein A-I/ApoA1 Antibody [NBP2-52979] - Western blot analysis using Apolipoprotein A-I/ApoA1 antibody. Harvested from mouse, separated on a 4-12 gradient gel by SDS-PAGE, transferred to PVDF membrane and blocked in 3% BSA/TBST. Probed with 1:8000 anti-apoA1 in 1%BSA/TBST, and detect edwith an anti-rabbit HRP secondary antibody using chemiluminescence. WB dilution 1: 8000, block before incubation overnight. Image from verified customer review.

Rabbit Polyclonal
Species Human, Mouse
Applications WB, Flow, ICC/IF

     1 Review

HEY2 Antibody - Azide and BSA Free
NBP3-03905
Western Blot: HEY2 Antibody [NBP3-03905] - Analysis of extracts of various cell lines, using HEY2 antibody at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB

GATD3A Antibody (1F5)
H00008209-M01
Western Blot: C21orf33 Antibody (1F5) [H00008209-M01] - C21orf33 monoclonal antibody (M01), clone 1F5 Analysis of C21orf33 expression in HeLa.Immunocytochemistry/Immunofluorescence: C21orf33 Antibody (1F5) [H00008209-M01] - Analysis of monoclonal antibody to C21orf33 on HeLa cell. Antibody concentration 10 ug/ml.

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


Related Genes

Alagille Syndrome has been researched against:

Related Pathways

Alagille Syndrome has been linked to:

Related Diseases

Alagille Syndrome has been studied in relation to diseases such as:

Related PTMs

Alagille Syndrome has been studied in relation to posttranslational modifications (PTMs) including:

Alternate Names

Alagille Syndrome is also known as alagille syndrome, hepatic ductular hypoplasia, arteriohepatic dysplasia, cholestasis with peripheral pulmonary stenosis, alagille-watson syndrome, cafe-au-lait macules with pulmonary stenosis, arteriohepatic dysplasia (disorder), arteriohepatic dysplasia (ahd), hypoplasia hepatic ductular, watson alagille syndrome, cholestasis, dysplasia.