anti rad1 Search Results


90
Boster Bio rad1
Western blot analyses of As –RAD9, As <t>–RAD1,</t> As –HUS1, As –RAD17, and As –CHK1 at different developmental stages (0 h–3 days) of A . sinica . ( A ) The intensities of the protein bands were normalized against those of GAPDH. ( B ) Values are expressed as arbitrary units of relative value. The x-axis indicates the different protein; the y-axis shows the relative expression level. Significant differences at different development stages ( P < 0.05) were analyzed by one-way analysis of variance (ANOVA) and reported by lowercase letters (a–e).
Rad1, supplied by Boster Bio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+rad1/pmc06826366-196-5-12?v=Boster+Bio
Average 90 stars, based on 1 article reviews
rad1 - by Bioz Stars, 2026-06
90/100 stars
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Rabbit anti-Human RAD1 Polyclonal Antibody
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This gene encodes a component of a heterotrimeric cell cycle checkpoint complex, known as the 9-1-1 complex, that is activated to stop cell cycle progression in response to DNA damage or incomplete DNA replication. The
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Boster Bio Anti-RAD1 Antibody catalog # A01396-1. Tested in IHC-P, WB applications. This antibody reacts with Human, Mouse.
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Rad1 antibody, 4.6 mg/ml (100 µl)
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RAD1 checkpoint DNA exonuclease, Recombinant Protein Epitope Signature Tag (PrEST) antigen sequence
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RAD1 Mouse anti-Human Monoclonal (N-Terminus) (Unconjugated) (4126) Antibody, (50 µg)
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Component of the 9-1-1 cell-cycle checkpoint response complex that plays a major role in DNA repair. The 9-1-1 complex is recruited to DNA lesion upon damage by the RAD17-replication factor C (RFC) clamp loader complex.
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Component of the 9-1-1 cell-cycle checkpoint response complex that plays a major role in DNA repair. The 9-1-1 complex is recruited to DNA lesion upon damage by the RAD17-replication factor C (RFC) clamp loader complex.
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Rabbit anti-Human RAD1 Polyclonal Antibody
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Image Search Results


Western blot analyses of As –RAD9, As –RAD1, As –HUS1, As –RAD17, and As –CHK1 at different developmental stages (0 h–3 days) of A . sinica . ( A ) The intensities of the protein bands were normalized against those of GAPDH. ( B ) Values are expressed as arbitrary units of relative value. The x-axis indicates the different protein; the y-axis shows the relative expression level. Significant differences at different development stages ( P < 0.05) were analyzed by one-way analysis of variance (ANOVA) and reported by lowercase letters (a–e).

Journal: Genes

Article Title: Investigation of the Possible Role of RAD9 in Post-Diapaused Embryonic Development of the Brine Shrimp Artemia sinica

doi: 10.3390/genes10100768

Figure Lengend Snippet: Western blot analyses of As –RAD9, As –RAD1, As –HUS1, As –RAD17, and As –CHK1 at different developmental stages (0 h–3 days) of A . sinica . ( A ) The intensities of the protein bands were normalized against those of GAPDH. ( B ) Values are expressed as arbitrary units of relative value. The x-axis indicates the different protein; the y-axis shows the relative expression level. Significant differences at different development stages ( P < 0.05) were analyzed by one-way analysis of variance (ANOVA) and reported by lowercase letters (a–e).

Article Snippet: Other antibodies, such as RAD17, RAD1, CHK1, and HUS1 were purchased from BOSTER (Wuhan, China) according to sequence homology, with all homology exceeding 80%.

Techniques: Western Blot, Expressing

Western blot analyses of As –RAD9, As –HUS1, As –RAD17, As –RAD1, and As –CHK1 proteins in response to temperature stresses. ( A ) The band intensity of the proteins is normalized to the band intensity of GAPDH. ( B ) The values are expressed as an arbitrary unit of relative value. Protein expression at 25 °C as control (blue), asterisk (**) indicates a statistical difference at P < 0.01, and (*) indicates 0.01 < P < 0.05.

Journal: Genes

Article Title: Investigation of the Possible Role of RAD9 in Post-Diapaused Embryonic Development of the Brine Shrimp Artemia sinica

doi: 10.3390/genes10100768

Figure Lengend Snippet: Western blot analyses of As –RAD9, As –HUS1, As –RAD17, As –RAD1, and As –CHK1 proteins in response to temperature stresses. ( A ) The band intensity of the proteins is normalized to the band intensity of GAPDH. ( B ) The values are expressed as an arbitrary unit of relative value. Protein expression at 25 °C as control (blue), asterisk (**) indicates a statistical difference at P < 0.01, and (*) indicates 0.01 < P < 0.05.

Article Snippet: Other antibodies, such as RAD17, RAD1, CHK1, and HUS1 were purchased from BOSTER (Wuhan, China) according to sequence homology, with all homology exceeding 80%.

Techniques: Western Blot, Expressing, Control

Western blot analyses of As –RAD9, As –RAD17, As –RAD1, and As –CHK1 proteins of A. sinica under different salt concentration stresses. ( A ) The band intensity of the protein is normalized to GAPDH. ( B ) The values are expressed as an arbitrary unit of relative value. The expression of the protein at a salinity of 28‰ as control (yellow), and asterisk (**) indicates a statistically significant difference of P < 0.01, and (*) indicates a 0.01 < P < 0.05.

Journal: Genes

Article Title: Investigation of the Possible Role of RAD9 in Post-Diapaused Embryonic Development of the Brine Shrimp Artemia sinica

doi: 10.3390/genes10100768

Figure Lengend Snippet: Western blot analyses of As –RAD9, As –RAD17, As –RAD1, and As –CHK1 proteins of A. sinica under different salt concentration stresses. ( A ) The band intensity of the protein is normalized to GAPDH. ( B ) The values are expressed as an arbitrary unit of relative value. The expression of the protein at a salinity of 28‰ as control (yellow), and asterisk (**) indicates a statistically significant difference of P < 0.01, and (*) indicates a 0.01 < P < 0.05.

Article Snippet: Other antibodies, such as RAD17, RAD1, CHK1, and HUS1 were purchased from BOSTER (Wuhan, China) according to sequence homology, with all homology exceeding 80%.

Techniques: Western Blot, Concentration Assay, Expressing, Control