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Anti-58K Golgi protein antibody [58K-9] - Golgi Marker
See all 58K Golgi protein products (7) ...
Mouse monoclonal [58K-9] to 58K Golgi protein - Golgi Marker
This product recognizes an epitope located on the microtubule-binding peripheral Golgi membrane 58 kDa protein.
WB, Functional Studies, ICC/IFmore details
Reacts with
Rat, Hamster, Dog, Human, Monkey, African Green Monkey
Predicted to work with
Cow, Pig
Full length native protein (purified) (Rat liver).
Rat Liver. For indirect immunofluorescence: cultured Chinese hamster ovary (CHO) cells For immunoblotting (colorimetric): whole rat liver extract Antigen M.W.: 58 kDa
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Store in the dark. Avoid repeated freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: PBS, pH 7.5
Concentration information loading...
IgG fraction
Monoclonal
58K-9
IgG1
Tags & Cell Markers >> Subcellular Markers >> Organelles >> Golgi
Signal Transduction >> Metabolism >> Amino Acids
Western blot - Anti-58K Golgi protein antibody [58K-9] - Golgi Marker (ab27043)
(enlarge)
Immunocytochemistry/ Immunofluorescence - Anti-58K Golgi protein antibody [58K-9] - Golgi Marker (ab27043)
(enlarge)
Immunocytochemistry/ Immunofluorescence - 58K Golgi protein antibody [58K-9] (ab27043)
(enlarge)
Our Abpromise guarantee covers the use of ab27043 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: Use a concentration of 1 - 5 µg/ml.Detects a band of approximately 58 kDa (predicted molecular weight: 58 kDa).
FuncS: Use at an assay dependent dilution.
ICC/IF: Use a concentration of 5 - 10 µg/ml.(Previous batches have worked at the concentration of 1µg/ml. Our current batch appears to work between 5 and 10 µg/ml. Please see the data below for more details.)
Folate-dependent enzyme, that displays both transferase and deaminase activity. Serves to channel one-carbon units from formiminoglutamate to the folate pool.
Binds and promotes bundling of vimentin filaments originating from the Golgi.
Amino-acid degradation; L-histidine degradation into L-glutamate; L-glutamate from N-formimidoyl-L-glutamate (transferase route): step 1/1.
One-carbon metabolism; tetrahydrofolate interconversion.
Defects in FTCD are the cause of glutamate formiminotransferase deficiency (FIGLU-URIA) [MIM:229100]; also known as formiminoglutamicaciduria (FIGLU-uria). It is an autosomal recessive disorder. Features of a severe phenotype, include elevated levels of formiminoglutamate (FIGLU) in the urine in response to histidine administration, megaloblastic anemia, and mental retardation. Features of a mild phenotype include high urinary excretion of FIGLU in the absence of histidine administration, mild developmental delay, and no hematological abnormalities.
In the C-terminal section; belongs to the cyclodeaminase/cyclohydrolase family.
In the N-terminal section; belongs to the formiminotransferase family.
Cytoplasm > cytoskeleton > centrosome > centriole. Golgi apparatus. More abundantly located around the mother centriole.
Target information above from: UniProt accessionO95954
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Anti-58K Golgi protein antibody [58K-9] - Golgi Marker (ab27043)
![Western blot - Anti-58K Golgi protein antibody [58K-9] - Golgi Marker (ab27043)](/ps/datasheet/images/27/ab27043/58K-Golgi-protein-Primary-antibodies-ab27043-4.jpg)
All lanes : Anti-58K Golgi protein antibody [58K-9] - Golgi Marker (ab27043) at 1 µg/ml
Lane 1 : Liver (Rat) Tissue Lysate, blocked with 5% BSA
Lane 2 : Liver (Rat) Tissue Lysate, blocked with 3% Milk
Lysates/proteins at 20 µg per lane.
Secondary
Goat polyclonal Secondary Antibody to Mouse IgG - H&L (HRP), pre-adsorbed (ab97040) at 1/5000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 58 kDa
Exposure time : 3 minutes
Abcam recommends using milk as the blocking agent. Abcam welcomes customer feedback and would appreciate any comments regarding this product and the data presented above.
Immunocytochemistry/ Immunofluorescence - Anti-58K Golgi protein antibody [58K-9] - Golgi Marker (ab27043)
![Immunocytochemistry/ Immunofluorescence - Anti-58K Golgi protein antibody [58K-9] - Golgi Marker (ab27043)](/ps/datasheet/images/27/ab27043/58K-Golgi-protein-Primary-antibodies-ab27043-9.jpg)
ab27043 (1µg/ml, 5µg/ml and 10µg/ml) staining 58K Golgi protein in SK-N-SH cells (green). Cells were fixed in Methanol, permabilised using 0.5% Triton X100 in PBS and counterstained with DAPI in order to highlight the nucleus (red).
Image courtesy of Dr. Kirk McManus, Univ. of Manitoba/Cancer Care MICB, Canada
Immunocytochemistry/ Immunofluorescence - 58K Golgi protein antibody [58K-9] (ab27043)
![Immunocytochemistry/ Immunofluorescence - 58K Golgi protein antibody [58K-9] (ab27043)](/ps/datasheet/Images/27/ab27043/ab27043-IF-Im3.jpg)
ICC/IF image of ab27043 stained human HeLa cells. The cells were methanol fixed (5 min) and incubated with the antibody (ab27043, 1µg/ml) for 1h at room temperature. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Image-iTTM FX Signal Enhancer was used as the primary blocking agent, 5% BSA (in TBS-T) was used for all other blocking steps. DAPI was used to stain the cell nuclei (blue). Alexa Fluor® 594 WGA was used to label plasma membranes (red).
This product has been referenced in:
See all 9 publications for this product
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![Western blot - Anti-58K Golgi protein antibody [58K-9] - Golgi Marker (ab27043)](/ps/datasheet/images/27/ab27043/58K-Golgi-protein-Primary-antibodies-ab27043-4.jpg)
All lanes : Anti-58K Golgi protein antibody [58K-9] - Golgi Marker (ab27043) at 1 µg/ml
Lane 1 : Liver (Rat) Tissue Lysate, blocked with 5% BSA
Lane 2 : Liver (Rat) Tissue Lysate, blocked with 3% Milk
Lysates/proteins at 20 µg per lane.
Secondary
Goat polyclonal Secondary Antibody to Mouse IgG - H&L (HRP), pre-adsorbed (ab97040) at 1/5000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 58 kDa
Exposure time : 3 minutes
Abcam recommends using milk as the blocking agent. Abcam welcomes customer feedback and would appreciate any comments regarding this product and the data presented above.
![Immunocytochemistry/ Immunofluorescence - Anti-58K Golgi protein antibody [58K-9] - Golgi Marker (ab27043)](/ps/datasheet/images/27/ab27043/58K-Golgi-protein-Primary-antibodies-ab27043-9.jpg)
ab27043 (1µg/ml, 5µg/ml and 10µg/ml) staining 58K Golgi protein in SK-N-SH cells (green). Cells were fixed in Methanol, permabilised using 0.5% Triton X100 in PBS and counterstained with DAPI in order to highlight the nucleus (red).
Image courtesy of Dr. Kirk McManus, Univ. of Manitoba/Cancer Care MICB, Canada
![Immunocytochemistry/ Immunofluorescence - 58K Golgi protein antibody [58K-9] (ab27043)](/ps/datasheet/Images/27/ab27043/ab27043-IF-Im3.jpg)
ICC/IF image of ab27043 stained human HeLa cells. The cells were methanol fixed (5 min) and incubated with the antibody (ab27043, 1µg/ml) for 1h at room temperature. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Image-iTTM FX Signal Enhancer was used as the primary blocking agent, 5% BSA (in TBS-T) was used for all other blocking steps. DAPI was used to stain the cell nuclei (blue). Alexa Fluor® 594 WGA was used to label plasma membranes (red).
![Anti-58K Golgi protein antibody [58K-9] - Golgi Marker for Immunocytochemistry/ Immunofluorescence in Human (27043)](/ps/datasheet/images/27/ab27043/58K-Golgi-protein-Primary-antibodies-ab27043-7.jpg)
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