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Rabbit Anti PSMB5 Polyclonal Affinity Purified (PBS with 0.02% sodium azide, 50% glycerol, pH7.3) (Western Blot,IHC,Immunofluorescence) from Innovative Research is a polyclonal antibody in a liquid format, buffered in PBS with 0.02% sodium azide, 50%
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Boster Bio
psmb5  Psmb5, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/anti+psmb5/Anti-PSMB5%2FMB1+Antibody+Picoband/pmc12818076-364-27-28 Average 94 stars, based on 1 article reviews
psmb5 - by Bioz Stars,
2026-10
94/100 stars
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The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits
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Recombinant Mouse Antibody scFv Fragment reacts with an antigen Human PSMB5, expressed in E. coli.Can be useful in applications such as: Western blot; Immunofluorescence; Functional Study4°C. For long term storage, aliquot and store at -20°C.
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Rabbit anti-Human PSMB5 Polyclonal Antibody
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Boster Bio Anti-Proteasome subunit beta type-5 PSMB5 Antibody catalog # A03418. Tested in WB,ICC/IF,IP applications. This antibody reacts with Human,Mouse,Rat.
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MB1 / PSMB5 Goat anti-Human Polyclonal (Unconjugated) Antibody, (50 µg)
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Recombinant Mouse Antibody Fab Fragment recognizes and reacts with Human PSMB5, expressed in Chinese Hamster Ovary cells(CHO).Can be useful in applications such as: Flow Cytometry; Western blot; Functional StudyStore at -20°C. Avoid multiple freeze/thaw cycles.http://www.creativebiolabs.net/Rcombinant-Anti-Human-PSMB5-Antibody-Fab-Fragment-9895.htm
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Detects proteasome PSMB5.The proteasome is a multicatalytic proteinase complex which is characterized by its ability to cleave peptides with Arg, Phe, Tyr, Leu, and Glu adjacent to the leaving group at neutral or slightly basic
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Rabbit anti-Human PSMB5 Polyclonal Antibody
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Image Search Results
Journal: iScience
Article Title: Ubiquitination and degradation of CD47 enhances macrophage phagocytosis of hemolytic erythrocytes
doi: 10.1016/j.isci.2025.114499
Figure Lengend Snippet: Changes in the major protein components of the proteasome during hemolysis (A) Western blot analysis of proteasomal subunits (PSME1/2, PSMB5/6/7) expression in control and hemolysis groups. (B and C) Quantification of proteasomal subunits (PSME1/2, PSMB5/6/7) expression in the RBC membrane (B) and cytoplasm (C) ( n = 3). (D) Representative immunofluorescence images of proteasomal subunits (PSME1/2, PSMB5/6/7) of hemolytic RBCs ( n = 6). Scale bars = 10 μm. (E) Schematic illustration of the animal model of immune hemolysis. (F and G) Immunofluorescence of proteasomal subunits (PSME1/2, PSMB5/6/7) in hemolytic mouse RBCs (F) and AIHA patient RBCs (G) ( n = 6). Scale bars = 10 μm. (H–J) Statistical analysis of caspase-like activity (H), trypsin-like activity (I), and chymotrypsin-like activity (J) of the membrane proteins after hemolysis ( n = 6). Data were analyzed by Student’s t test (two groups) or one-way ANOVA with Tukey’s test (multiple groups) and are expressed as mean ± SEM. ∗ p < 0.05, ∗∗∗ p < 0.001, ns = no significance.
Article Snippet: The primary antibodies utilized in this procedure were CD47 (Santa Cruz Biotechnology, Cat# sc-12730), MARCH1 (HUABIO Biotechnology, Cat# ER63906), PSME1 (Abcam, Cat# ab186832), PSME2 (Abcam, Cat# ab183727),
Techniques: Western Blot, Expressing, Control, Membrane, Immunofluorescence, Animal Model, Activity Assay