ebioscience Phospho-MCL-1 (Ser159) Monoclonal Antibody (RBCERNR), PE,Phospho-MCL-1 (Ser159) Monoclonal Antibody (RBCERNR), PE

2024-10-23

Phospho-MCL-1 (Ser159) Monoclonal Antibody (RBCERNR), PE

货号:12-9038-42

规格:100 Tests

价格:3513

产品类型:流式抗体

品牌:eBioscience

物种:人/小鼠

宿主:小鼠

抗体亚型:IgG2b, kappa

克隆号:RBCERNR

荧光染料:PE

类型:单抗同型对照:Mouse IgG2b kappa Isotype Control (eBMG2b), PE
浓度:5 µL/Test用法:5 µL (0.125 µg)/test(Flow)
产品详细信息Description: This RBCERNR monoclonal antibody recognizes human and mouse myeloid cell leukemia sequence 1 (Mcl-1) when phosphorylated on serine 159 (S159). Mcl-1 is an anti-apoptotic protein that is a member of the Bcl-2 family of proteins important for regulation of cell survival/apoptosis. Mcl-1 is primarily localized to the outer membrane of mitochondria where it prevents cytochrome c release via dimerization with other Bcl-2 family members such as Bim. PI3K activation of AKT results in the phosphorylation of GSK3 beta at serine 9 (S9) resulting in destabilization and degradation of GSK3 beta. Loss of GSK3 beta prevents phosphorylation of Mcl-1 on S159 and its subsequent ubiquitnation and degradation. Mice conditionally lacking Mcl-1 in lymphocytes showed that Mcl-1 is essential during early lymphoid development and for the maintenance of mature lymphocytes.Applications Reported: This RBCERNR antibody has been reported for use in intracellular staining followed by flow cytometric analysis.Applications Tested: This RBCERNR antibody has been pre-titrated and tested by intracellular staining followed by flow cytometric analysis of normal human peripheral blood cells. This can be used at 5 µL (0.125 µg) per test. A test is defined as the amount (µg) of antibody that will stain a cell sample in a final volume of 100 µL. Cell number should be determined empirically but can range from 10^5 to 10^8 cells/test.Staining Protocol: Protocol A and Protocol C are recommended for this monoclonal antibody. Use of Protocol A: Two-step protocol: intracellular (cytoplasmic) proteins allows for the greatest flexibility for detection of surface and intracellular (cytoplasmic) proteins. Protocol C: Two-step protocol: Fixation/Methanol allows for the greatest discrimination of phospho-specific signaling between unstimulated and stimulated samples, but with limitations on the ability to stain specific surface proteins (refer to "Clone Performance Following Fixation/Permeabilization" located in the Best Protocols Section under the Resources tab online). All Protocols can be found in the Flow Cytometry Protocols: "Staining Intracellular Antigens for Flow Cytometry Protocol" located in the Best Protocols Section under the Resources tab online.Excitation: 488-561 nm; Emission: 578 nm; Laser: Blue Laser, Green Laser, Yellow-Green Laser.Filtration: 0.2 µm post-manufacturing filtered.靶标信息MCL1 (Myeloid cell leukemia-1) belongs to the Bcl-2 family and is involved in programing, differentiation and concomitant maintenance of cell viability, but not of proliferation. Isoform 1 of MCL1 inhibits apoptosis while isoform 2 promotes it. The carboxy terminal of MCL1 and bcl-2 share significant sequence homology. Expression of MCL1 is increased upon exposure of ML-1 cells to various types of DNA damaging agents (e.g. ionizing radiation, ultraviolet radiation, and alkylating drugs) along with increases in GADD45 and Bax and a decrease in bcl-2. Enhanced expression of MCL1, prominently associated with mitochondria, complements the continued expression of bcl-2 in ML-1 cells undergoing differentiation. Like bcl-2, MCL1 has the capacity to promote cell viability under conditions that otherwise cause apoptosis. While the mechanism by which MCL1 inhibits apoptosis is not known, it is thought that it may heterodimerize and neutralize pro-apoptotic members of the Bcl-2 family such as Bim or Bak. MCL1 was originally identified in differentiating myeloid cells, but has since been shown to be expressed in multiple cell types. MCL1 is essential for embryogenesis and for the development and maintenance of B and T lymphocytes in animals. MCL1 exists as at least two distinct isoforms designated MCL1L and MCL1S. In marked contrast to the larger isoform of MCL1, overexpression of MCL1S promotes cell death.
数据
Phospho-MCL-1 (Ser159) Antibody (12-9038-42) in FlowTOP: Intracellular staining of normal human peripheral blood cells that were untreated (left) or treated with Calyculin A for 4 hours (right) with Anti-Human CD3 PerCP-Cyanine5-5 (Product # 45-0036-42) and phospho-Mcl-1 (S159) PE. Plots show cells in the lymphocyte gate. BOTTOM: Normal human peripheral blood cells were unstimulated (orange histogram), were stimulated with Anti-Human CD3 and CD28 Functional Grade Purifieds (Product # 16-0037-81andProduct # 16-0289-81) in the presence of the proteasome inhibitor MG-132 (purple histogram), or were treated with Calyculin A (green histogram). The cells were then intracellularly stained with Anti-Human CD3 PerCP-Cyanine5-5 (Product # 45-0036-42) and Anti-Human/Mouse phospho-Mcl-1 (S159) PE using the Intracellular Fixation and Permeabilization Buffer Set (Product # 88-8824-00) and protocol. CD3+ cells in the lymphocyte gate were used for analysis.
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