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. 2015 Jan 28;308(7):R636–R649. doi: 10.1152/ajpregu.00489.2014

Table 1.

Working dilutions and immunoblot buffers of the employed antibodies

Antibody Supplier Dilution Blocking Buffer Antibody Incubation Buffer
Primary antibodies
    phospho-AMPKα (Thr-172) (40H9); rabbit Cell Signaling 1:1000 5 % BSA/TBST 50 mM NaF 5 % BSA/TBST 50 mM NaF
    AMPKα (23A3); rabbit Cell Signaling 1:1000 5 % BSA/TBST 5 % BSA/TBST
    phospho-CREB (Ser-133); rabbit Biotrend/Signalway 1:4000 3 % BSA/TBST 50 mM NaF 3 % BSA/TBST 50 mM NaF
    CREB (Ab-129); rabbit Biotrend/Signalway 1:4000 3 % milk/TBST 50 mM NaF 3 % milk/TBST 50 mM NaF
    CBS monoclonal (M01), clone 3E1; mouse Abnova 1:1000 5 % milk/PBST 5 % milk/PBST
    CSE monoclonal (M03), clone  S51; mouse Abnova 1:1000 5 % milk/PBST 5 % milk/PBST
    α-tubulin; mouse Sigma 1:3000–1:10000 3–5 % milk/TBST 3–5% milk/TBST
Secondary HRP-linked antibodies
    anti-rabbit IgG Cell Signaling 1:3000 n/a primary antibody buffer
    anti-mouse IgG Thermo Scientific 1:3000 n/a primary antibody buffer

TBST, Tris-buffered saline containing 1 % Tween-20; PBST, phosphate-buffered saline containing 1% Tween-20; BSA, bovine serum albumin; CSE, cystathionine-γ-lyase.