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mouse anti hcr1 moab  (R&D Systems)


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    R&D Systems mouse anti hcr1 moab
    Mouse Anti Hcr1 Moab, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+cripto+1/Human%2FPrimate+Cripto-1+Antibody/pmc11545644-95-2-0
    Average 92 stars, based on 1 article reviews
    mouse anti hcr1 moab - by Bioz Stars, 2026-11
    92/100 stars

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    Related Articles

    other:

    Article Title: Exosomal Cripto-1 Serves as a Potential Biomarker for Perihilar Cholangiocarcinoma
    Article Snippet: The following primary antibodies were used: Cripto-1 Antibody (R&D, MAB2772, 1:100 dilution), Ki-67 (CST, #9027, 1:400 dilution), E-Cadherin (CST, #3195, 1:400 dilution).

    Article Title: Cripto-1 overexpression is involved in the tumorigenesis of gastric-type and pancreatobiliary-type intraductal papillary mucinous neoplasms of the pancreas
    Article Snippet: The primary antibodies used were: anti-Cripto-1 (89646, monoclonal, R&D systems, Minneapolis, USA; 1:200 dilution), anti-MUC1 (Ma552, monoclonal, Novocastra Laboratories, Newcastle upon Tyne, UK; 1:200 dilution) and anti-MUC2 (H-300, polyclonal, Santa Cruz Biotechnology, Santa Cruz, CA, USA; 1:200 dilution).

    Article Title: Human Cripto-1 and Cripto-3 Protein Expression in Normal and Malignant Settings That Conflicts with Established Conventions
    Article Snippet: R&D Systems mouse anti-hCR1 MoAb (Cat# MAB 2772, Lot# VABO 0117121).



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    Selected validation of Nanostring gene expression analysis by qRT-PCR. Four genes including <t>CR1,</t> FOXD3, WNT3, and NOTCH4 are shown here as representatives for amplification. Data are the average of 8 samples from SFN pre-treated group and 8 samples from saline control. All experiments were conducted in duplicates. *: P < 0.05 as compared to the control animals.
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    Selected validation of Nanostring gene expression analysis by qRT-PCR. Four genes including CR1, FOXD3, WNT3, and NOTCH4 are shown here as representatives for amplification. Data are the average of 8 samples from SFN pre-treated group and 8 samples from saline control. All experiments were conducted in duplicates. *: P < 0.05 as compared to the control animals.

    Journal: Cancer prevention research (Philadelphia, Pa.)

    Article Title: Sulforaphane suppresses the growth of triple-negative breast cancer stem-like cells in vitro and in vivo

    doi: 10.1158/1940-6207.CAPR-18-0241

    Figure Lengend Snippet: Selected validation of Nanostring gene expression analysis by qRT-PCR. Four genes including CR1, FOXD3, WNT3, and NOTCH4 are shown here as representatives for amplification. Data are the average of 8 samples from SFN pre-treated group and 8 samples from saline control. All experiments were conducted in duplicates. *: P < 0.05 as compared to the control animals.

    Article Snippet: CR1 (R&D Systems, Cat# 145-CR/CF), Nodal (R&D Systems, Cat# 3218-ND-024/CF), GRP78 (Abcam, Cat# ab78432), and Alk4 (Creative BioMart, Cat# ACVR1B-645H,) were purchased from the indicated vendors.

    Techniques: Biomarker Discovery, Gene Expression, Quantitative RT-PCR, Amplification, Saline, Control

    ELISA assessment of CR1 binding to solid phase BPs including Nodal, GRP78, and Alk4 in the absence (-S) or presence (+S) of 100µM of SFN. CR1 binding to individual BPs in the absence of SFN (-S) condition was normalized to 100%. Percentage reaction induced CR1 binding inhibition was then determined using the 100% reference point for respective BPs. Data represents average values determined from three separate studies with samples run in octuplicate.

    Journal: Cancer prevention research (Philadelphia, Pa.)

    Article Title: Sulforaphane suppresses the growth of triple-negative breast cancer stem-like cells in vitro and in vivo

    doi: 10.1158/1940-6207.CAPR-18-0241

    Figure Lengend Snippet: ELISA assessment of CR1 binding to solid phase BPs including Nodal, GRP78, and Alk4 in the absence (-S) or presence (+S) of 100µM of SFN. CR1 binding to individual BPs in the absence of SFN (-S) condition was normalized to 100%. Percentage reaction induced CR1 binding inhibition was then determined using the 100% reference point for respective BPs. Data represents average values determined from three separate studies with samples run in octuplicate.

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    Techniques: Enzyme-linked Immunosorbent Assay, Binding Assay, Inhibition