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Negative Regulation Of Centriole Replication Pathway Bioinformatics

Disease and disorder research has been conducted in relation to the Negative Regulation Of Centriole Replication Pathway and Liver Carcinoma, Hepatitis, Hepatitis B, Hepatitis C, Carcinoma. The study of the Negative Regulation Of Centriole Replication Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Negative Regulation Of Centriole Replication Pathway has been researched in relation to Negative Regulation Of Wnt Receptor Signaling Path, Induction Of Apoptosis, Negative Regulation Of Peptidase Activity, Centriole Replication, Signal Transduction By P53 Class Mediator. The Negative Regulation Of Centriole Replication Pathway complements our catalog of research reagents including antibodies and ELISA kits against DKK1, PHLDA2, BUB1B, CSTB, CST6.

Negative Regulation Of Centriole Replication 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 Negative Regulation Of Centriole Replication below! For more information on how to use Laverne, please read the How to Guide.
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Top Research Reagents

We have 487 products for the study of the Negative Regulation Of Centriole Replication Pathway that can be applied to Chromatin Immunoprecipitation, Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.

NB100-1347
Immunohistochemistry-Paraffin: TSSC3 Antibody [NB100-1347] - Staining of paraffin embedded Human Placenta. Antibody at 3.75 ug/mL. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.Immunohistochemistry-Paraffin: TSSC3 Antibody [NB100-1347] - Staining of paraffin embedded Human Prostate. Antibody at 3.75 ug/mL. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.

Goat Polyclonal
Species Human
Applications IHC, IHC-P, PEP-ELISA

1 Publication
NB100-598
Western Blot: BRCA1 Antibody (RAY) [NB100-598] - Analysis of BRCA1 on MCF7 lysate.Immunocytochemistry/Immunofluorescence: BRCA1 Antibody (RAY) [NB100-598] - BRCA (RAY) antibody was tested in MCF-7 cells with FITC (green). Nuclei and alpha-tubulin were counterstained with DAPI (blue) and DyLight 550 (red).

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

4 Publications
NB100-353
Western Blot: BubR1 Antibody (8G1) [NB100-353] - BUBR1 detected in HeLa cell lysate using NB 100-353.Immunocytochemistry/Immunofluorescence: BubR1 Antibody (8G1) [NB100-353] - Immunofluorescence of an asynchronous cycling population of human cells (U2OS) with NB100-353. No signal is detected from interphase cells, whereas cells undergoing mitosis accumulate BubR1 at the kinetochores. Image reveals kinetochores at prometaphase. Image courtesy of Luke Hughes-Davies and Rhiannon Jade, Gurdon Institute, Cambridge, UK.

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

     1 Review

8 Publications
NBP2-35224
SDS-Page: Human PTHLH/PTHrP Protein [NBP2-35224]


Species Human
Applications Func, PAGE

AF1120
Frizzled‑1 was detected in immersion fixed frozen sections of embryonic mouse intestine (13 d.p.c.) using 15 µg/mL Goat Anti-Mouse Frizzled‑1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1120) overnight at <BR>4 °C. Tissue was stained with the Anti-Goat HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # <A class=NoLineLink href=

Goat Polyclonal
Species Mouse
Applications WB, IHC

3 Publications
AF1408
Western blot shows lysates of human colon tissue, PC‑12 rat adrenal pheochromocytoma cell line, A549 human lung carcinoma cell line, and SK‑BR‑3 human breast cancer cell line. PVDF membrane was probed with 1 µg/mL of Goat Anti-Human/Rat Cystatin B Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1408) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # <A class=NoLineLink href=    Western  blot shows lysates of HEK293T human embryonic kidney parental cell line and  Cystatin B knockout HEK293T cell line (KO). PVDF membrane was probed with  1 µg/mL of Goat Anti-Human/Rat Cystatin B Antigen  Affinity-purified Polyclonal Antibody (Catalog # AF1408) followed by  HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # <a class=

Goat Polyclonal
Species Human, Rat
Applications WB, Simple Western, IHC

2 Publications
AF1286
    Western  blot shows lysates of human skin tissue. PVDF membrane was probed with  1 µg/mL of Goat Anti-Human Cystatin E/M Antigen  Affinity-purified Polyclonal Antibody (Catalog # AF1286) followed by  HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # <a class=    Simple  Western lane view shows lysates of human skin tissue, loaded at  0.2 mg/mL. A specific band was detected for Cystatin E/M at  approximately 13 kDa (as indicated) using 50 µg/mL of Goat  Anti-Human Cystatin E/M Antigen Affinity-purified Polyclonal  Antibody (Catalog # AF1286) followed by 1:50 dilution of HRP-conjugated  Anti-Goat IgG Secondary Antibody (Catalog # <a class=

Goat Polyclonal
Species Human
Applications WB, Simple Western, IHC

     1 Review

4 Publications
AF1617

Goat Polyclonal
Species Human
Applications WB

7 Publications
5439-DK/CF
<P align=left>1 μg/lane of Recombinant Human Dkk-1 was resolved with SDS-PAGE under reducing (R) conditions and visualized by silver staining, showing major bands at 33-38 kDa. Multiple bands in gel are due to variable glycosylation.</P>Recombinant  Human Wnt‑3a (Catalog # <a class=


Species Human
Applications BA

70 Publications
1109-N1/CF
<P align=left>1 μg/lane of Recombinant Mouse Netrin-1 was resolved with SDS-PAGE under reducing (R) conditions and visualized by silver staining, showing a band at 83 kDa.


Species Mouse
Applications Bind

29 Publications

Related Genes

The Negative Regulation Of Centriole Replication Pathway has been researched against:

Related Diseases

The Negative Regulation Of Centriole Replication Pathway has been studied in relation to diseases such as:

Related PTMs

The Negative Regulation Of Centriole Replication Pathway has been studied in relation to posttranslational modifications (PTMs) including: