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csk  (Proteintech)


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    Structured Review

    Proteintech csk
    Csk, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/csk/CSK+Antibody/pm41462160-155-2-14
    Average 93 stars, based on 8 article reviews
    csk - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    other:

    Article Title: PEAK1 maintains tight junctions in intestinal epithelial cells and resists colitis by inhibiting autophagy-mediated ZO-1 degradation
    Article Snippet: CSK (Proteintech, Cat# 17720-1-AP) 11.

    Western Blot:

    Article Title: Crk mediates Csk-Hippo signaling independently of Yap tyrosine phosphorylation to induce cell extrusion
    Article Snippet: Antibodies against phospho-Tyrosine (P-Tyr-100) (CST #9411), YAP (CST #14074 and Santa Cruz #sc-271134), and Flag (CST # 8146) were used for immunoprecipitation (5 μg antibody for 500 μg protein). .. Antibodies against Crk (BD #610036), Csk (Proteintech #17720-AP), ERK1/2 (CST #4695), pCRK (CST #3491), pERK1/2 (Santa Cruz Biotechnology, sc-7383), pSRC416 (CST #6943), pSRC527 (CST #2105), YAP (CST #14074), and phospho-tyrosine (P-Tyr-100) #9411 were used in western blot (1:1000 dilution). .. The plasmid encoding wild-type Yap was obtained from Addgene (pcDNA Flag Yap1, Addgene #18881).



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    Image Search Results


    Six-weeks-old C57BL/6 male mice were mock-transduced or transduced with 10 11 ⍰vge of AAV-HBV 1.3 mer genotype D/serotype ayw for 31 days to allow establishment of chronic infection. At day-35, treatment cycles were started, after mice were evenly grouped according to viremia and HBsAg antigenemia. Mice (n⍰= ⍰7/group) were injected, at indicated days with vehicle (PBS), free/non vectorized Pam 3 CSK 4 at 100 μg/injection, NP-Pam 3 CSK 4 at 5 μg/shot, or NP-Pam 3 CSK 4 at 20 μg/shot. 3TC was administrated continously at approximately 100 mg/kg/day (in drinking water) between days-35 and 64 and days-79 and 90. Blood/serum was collected at indicated times (blood drop symbol). Mice were euthanized at 90 days post-transduction. The different readouts and used techniques for exploitation of blood and liver samples are indicated.

    Journal: bioRxiv

    Article Title: Preclinical antiviral study of a liver-targeted TLR1/2 agonist in an immune-competent mouse model of HBV infection

    doi: 10.64898/2026.05.27.728102

    Figure Lengend Snippet: Six-weeks-old C57BL/6 male mice were mock-transduced or transduced with 10 11 ⍰vge of AAV-HBV 1.3 mer genotype D/serotype ayw for 31 days to allow establishment of chronic infection. At day-35, treatment cycles were started, after mice were evenly grouped according to viremia and HBsAg antigenemia. Mice (n⍰= ⍰7/group) were injected, at indicated days with vehicle (PBS), free/non vectorized Pam 3 CSK 4 at 100 μg/injection, NP-Pam 3 CSK 4 at 5 μg/shot, or NP-Pam 3 CSK 4 at 20 μg/shot. 3TC was administrated continously at approximately 100 mg/kg/day (in drinking water) between days-35 and 64 and days-79 and 90. Blood/serum was collected at indicated times (blood drop symbol). Mice were euthanized at 90 days post-transduction. The different readouts and used techniques for exploitation of blood and liver samples are indicated.

    Article Snippet: Either Pam 3 CSK 4 (InvivoGen, USA) or the near-infrared fluorescent probe DiR XenoLight Dye (λ excitation = 750 nm, λ emission = 770 nm) (Perkin Elmer, USA) was incorporated during the nanoprecipitation.

    Techniques: Transduction, Infection, Injection