Bs 3602r

Manufactured by Bioss Antibodies

The Bs-3602R is a laboratory centrifuge designed for high-speed separation of samples. It features a maximum speed of 6,000 rpm and a maximum relative centrifugal force (RCF) of 3,602 x g. The centrifuge can accommodate a variety of rotor types and sample volumes, making it suitable for a wide range of applications in research and diagnostic laboratories.

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Lab products found in correlation

Abp53067, by Abbkine (3 mentions) Bs 23779r, by Bioss Antibodies (3 mentions) Nb100 2220, by Novus Biologicals (3 mentions) Pa5 17564, by Thermo Fisher Scientific (2 mentions) Hs201 01, by Transgene (2 mentions) Hs101 01, by Transgene (2 mentions) Af519, by Beyotime (2 mentions) Bs 1115r, by Bioss Antibodies (1 mentions) Ab32096, by Abcam (1 mentions) Anti fasn, by Proteintech (1 mentions) Anti pc gtx132002, by GeneTex (1 mentions) A01030, by Abbkine (1 mentions) Proteinfind goat anti mouse igg, by Transgene (1 mentions) Proteinfind goat anti rabbit igg, by Transgene (1 mentions) Gtx112898, by GeneTex (1 mentions) Bs 1064r, by Bioss Antibodies (1 mentions)

3 protocols using bs 3602r

Western Blot Analysis of Muscle Proteins

Cited 1 time

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Western blot analysis was performed as previously described.⁶⁶ (link) The primary antibodies used were anti-FLAG (AF519, Beyotime, 1:1,000), anti-MYOD (ABP53067, Abbkine, 1:500), anti-MyHC (B103, DHSB, 0.5 μg/mL), anti-SERCA2 (NB100-237, Novus, 1:2,000), anti-ACC (PA5-17564, Thermo Fisher Scientific, 1:1,000), anti-pACCSer80 (orb315750, Biorbyt, 1:500), anti-CPT1 (bs-23779R, Bioss, 1:500), anti-pmTORSer2488 (#5536, CST, 1:1,000), anti-mTOR (bs-1992R, Bioss, 1:500), anti-ULK1 (bs-3602R, Bioss, 1:500), anti-LC3B (NB100-2220, Novus, 2.0 μg/mL), anti-P62 (18420-1-AP, Proteintech, 1:1,000), anti-CREB (bs-0035R, Bioss, 1:500), anti-pCREBSer133 (ab32096, Abcam, 1:5,000), anti-AMPK (bs-1115R, Bioss, 1:500), anti-pAMPKser712 (ABN-PAB12602, Abnova, 1:2,000), anti-Calcineurin (#2614S, CST, 1:1,000), anti-PGC-1α (66369-1-Ig, Proteintech, 1:5,000), and anti-GAPDH (60004-1-Ig, Proteintech, 1:5,000). ProteinFind goat anti-mouse IgG(H+L), HRP conjugate (HS201-01, TransGen, 1:1,000) and ProteinFind goat anti-rabbit IgG(H+L), HRP conjugate (HS101-01, TransGen, 1:500) were used as secondary antibodies.

Cai B., Ma M., Zhang J., Wang Z., Kong S., Zhou Z., Lian L., Zhang J., Li J., Wang Y., Li H., Zhang X, & Nie Q. (2021). LncEDCH1 improves mitochondrial function to reduce muscle atrophy by interacting with SERCA2. Molecular Therapy. Nucleic Acids, 27, 319-334.

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Western Blot and Immunofluorescence Analysis

Cited 1 time

Check if the same lab product or an alternative is used in the 5 most similar protocols

Western blots were performed as previously described [50 (link)]. The primary antibodies used were anti-FLAG (AF519, 1:1,000, Beyotime), anti-ACACA (PA5-17564, 1:1000, Thermo Fisher Scientific), anti-p-ACACA Ser⁸⁰ (orb315750, 1:500, Biorbyt), anti-PC (GTX132002, 1:500, GeneTex), anti-MYOD (ABP53067, 1:500, Abbkine), anti-MyHC (B103, 0.5 μg/ml, DHSB), anti-CPT1 (bs-23779R, 1:500, Bioss), anti-FASN (10624-2-AP, 1:200, Proteintech), anti-p-mTOR Ser²⁴⁸⁸ (#5536, 1:1000, CST), anti-mTOR (bs-1992R, 1:500; Bioss), Ubiquitin (#39361:1000, CST) anti-ULK1 (bs-3602R, 1:500; Bioss), anti-LC3B (NB100-2220, 2.0 ug/ml, Novus), anti-P62 (18420-1-AP, 1:1000, Proteintech) and anti-β-Tubulin (A01030, 1:10000, Abbkine). ProteinFind Goat Anti-Mouse IgG(H + L), HRP Conjugate (HS201-01, 1:1,000, TransGen) and ProteinFind Goat Anti-Rabbit IgG(H + L), HRP Conjugate (HS101-01, 1:500, TransGen) were used as a secondary antibody.
Immunofluorescence was performed using anti-MyHC (B103, 2.5 μg/ml, DHSB), as previously described [50 (link)]. A fluorescence microscope ((DMi8; Leica, German) was used to capture three randomly selected fields to visualize the area labeled with anti-MyHC.

Cai B., Ma M., Zhang J., Kong S., Zhou Z., Li Z., Abdalla B.A., Xu H., Zhang X., Lawal R.A, & Nie Q. (2022). Long noncoding RNA ZFP36L2-AS functions as a metabolic modulator to regulate muscle development. Cell Death & Disease, 13(4), 389.

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Western Blot Analysis of Muscle Proteins

Check if the same lab product or an alternative is used in the 5 most similar protocols

Western blot analysis was performed as previously described [44 (link)]. The primary antibodies used were anti-FLAG (AF519, Beyotime,1:1,000), anti-MYOD (ABP53067, Abbkine, 1:500), anti-MyHC (B103, DHSB, 0.5 mg/mL), anti-FASN (10624-2-AP, Proteintech, 1:200), anti-CPT1 (bs-23779R, Bioss, 1:500), anti-ULK1 (bs-3602R, Bioss,1:500), anti-LC3B (NB100-2220, Novus, 2.0 mg/mL), anti-P62 (18420-1-AP, Proteintech, 1:1,000), anti-TBP (44059, Cell signaling, 1:1000), anti-KLF4 (bs-1064R, Bioss,1:500), anti-GPI (GTX113203, GeneTex, 1:500), anti-TNNI2 (bs-10617R, Bioss, 1:500), anti-CDKN1A (GTX112898, GeneTex, 1:500), and anti-GAPDH (60004-1-Ig, Proteintech, 1:5,000). ProteinFind goat anti-mouse IgG(H + L), HRP conjugate (HS201-01, TransGen, 1:1,000) and ProteinFind goat anti-rabbit IgG(H + L), HRP conjugate (HS101-01, TransGen, 1:500) were used as secondary antibodies. The original images of western blot are shown in Additional file 1.

Ma M., Cai B., Zhou Z., Kong S., Zhang J., Xu H., Zhang X, & Nie Q. (2023). LncRNA-TBP mediates TATA-binding protein recruitment to regulate myogenesis and induce slow-twitch myofibers. Cell Communication and Signaling : CCS, 21, 7.

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