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- Antibody Data
- Antigen structure
- References [1]
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- Validations
- Western blot [1]
- Immunocytochemistry [1]
- Immunohistochemistry [1]
- Other assay [1]
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- Product number
- PA5-56448 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- LYRM4 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Recombinant full-length protein
- Description
- Immunogen sequence: RAMLRESKRF SAYNYRTYAV RRIRDAFREN KNVKDPVEIQ TLVNKAKRDL GVIRRQVHIG QLYSTDKLII ENRD
- Concentration
- 0.3 mg/mL
Submitted references Mitochondrial fatty acid synthesis coordinates oxidative metabolism in mammalian mitochondria.
Nowinski SM, Solmonson A, Rusin SF, Maschek JA, Bensard CL, Fogarty S, Jeong MY, Lettlova S, Berg JA, Morgan JT, Ouyang Y, Naylor BC, Paulo JA, Funai K, Cox JE, Gygi SP, Winge DR, DeBerardinis RJ, Rutter J
eLife 2020 Aug 17;9
eLife 2020 Aug 17;9
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of LYRM4 in control (vector only transfected HEK293T lysate) and LYRM4 over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (~3.1 kDa) in mammalian HEK293T cells). Samples were probed using a LYRM4 Polyclonal Antibody (Product # PA5-56448).
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunofluorescent staining of LYRM4 in human cell line U-251 MG shows positivity in nucleus. Samples were probed using a LYRM4 Polyclonal Antibody (Product # PA5-56448).
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunohistochemical staining of LYRM4 in human hippocampus shows strong cytoplasmic positivity in neuronal cells. Samples were probed using a LYRM4 Polyclonal Antibody (Product # PA5-56448).
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Figure 3. Posttranslational loss of ETC components in mtFAS mutants is specific to LYR proteins and their targets. ( A-B ) Duplicate samples from the indicated cell lines were grown under proliferative conditions and subjected to TMT labeling and quantitative proteomics analysis. ( A ) Volcano plot of compiled Mecr clones vs. GFP controls showing all proteins (gray), mitochondrial proteins (blue), and electron transport chain subunits (ETC, red). Dashed gray lines indicate cutoffs for significance at -log10(p-value) = 1.3 and log2(Fold Change) = +/- 0.59. ( B ) Heatmap depicting log 2 (Fold Change) of OXPHOS subunits in the indicated cell lines. ( C ) Quadruplicate samples from mtFAS mutant cells and controls were grown under proliferative conditions. Total RNA was isolated, used as input for mRNA library prep, and sequenced. Resulting data were aligned to the mouse genome and analyzed for differential expression. ETC subunit-encoding transcripts are shown in red vs. all other transcripts (gray). ( D-G ) Relative abundance of the indicated LYR proteins or their targets in the indicated cell lines from the quantitative proteomics experiment described in ( A-B ) #=p < 0.01, +=p < 0.001, ++=p < 0.0001, error bars are SD. All statistical comparisons shown are between mtFAS mutants and GFP-1 clone; p-values when compared with GFP-2 clone were similar or smaller than when compared with GFP-1 clone. ( H ) Crude mitochondrial lysates generated from the indicated cell lines by differe
