HL-60 whole cell lysate
HL-60 whole cell lysate
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(4 Publications)
- WB
Project1671****
Western blot - HL-60 whole cell lysate (AB7914)
ab26483 consistently detects a band at 55-60 kDa but we also see bands of ~35 and 70 kDa that appear with varying intensity in some of our extracts. We cannot find an explanation for this and are unsure of the nature of these crossreacting bands.
All lanes:
Western blot - Anti-Cdc20 antibody (<a href='/products/primary-antibodies/cdc20-antibody-ab26483'>ab26483</a>) at 1 µg/mL
Lane 1:
Raji (Human Burkitt's lymphoma cell line) Whole Cell Lysate (ab7908) at 20 µg
Lane 2:
Western blot - THP-1 whole cell lysate (<a href='/products/cell-lysates/thp-1-whole-cell-lysate-ab7913'>ab7913</a>) at 20 µg
Lane 3:
Western blot - HEK-293 whole cell lysate (<a href='/products/cell-lysates/hek-293-whole-cell-lysate-ab7902'>ab7902</a>) at 20 µg
Lane 4:
Western blot - HL-60 whole cell lysate (ab7914) at 20 µg
Secondary
All lanes:
IRDye 680 Conjugated Goat Anti-Rabbit IgG (H+L) at 1/15000 dilution
Predicted band size: 55 kDa
false
Reactivity data
製品の詳細
Cell line: HL60 (Human promyelocytic leukemia).
Growth media: RPMI and 10% FBS (Fetal bovine serum).
HL60 cell lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl flouride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 µg/ml of aprotinin, 5 µg/ml of leupeptin). Cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The cell lysate was boiled for 5 min in 1 x SDS sample buffer (0.045 M Tris-HCl pH 6.8, 10% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue), containing 0.05 M DTT.
出荷温度及び保存条件
出荷温度
長期保存温度
分注に関する情報
保管に関する情報
Cell culture
文献 (4)
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International journal of molecular sciences 25: PubMed39273253
2024
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Cells 12: PubMed37887347
2023
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PloS one 18:e0286278 PubMed37874822
2023
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American journal of respiratory cell and molecular 40:200-10 PubMed18703796
2008
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