Anti-IL-6 antibody [RM1304]
- BOND RX™ Validated
- RabMAb
- Recombinant
- 20ul selling size
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Rabbit Recombinant Multiclonal IL-6 antibody. Suitable for WB, IHC-P and reacts with Human, Mouse samples.
View Alternative Names
IFNB2, IL6, Interleukin-6, IL-6, B-cell stimulatory factor 2, CTL differentiation factor, Hybridoma growth factor, Interferon beta-2, BSF-2, CDF, IFN-beta-2, Il-6, Il6, Interleukin-6, IL-6, B-cell hybridoma growth factor, Interleukin HP-1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-6 antibody [RM1304] (AB324449)
Immunohistochemical analysis of paraffin-embedded Image A U-87 MG (human glioblastoma-astrocytoma epithelial cell) cell pellets treated with 1ug/ml Lipopolysaccharide (LPS) and 300ng/ml Brefeldin A for 16 hours Image B Untreated U-87 MG cell pellets tissue labeling IL-6 with ab324449 at 1/200 (2.585 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Cytoplasmic staining on TU-87 MG (human glioblastoma-astrocytoma epithelial cell) cell pellets treated with 1ug/ml Lipopolysaccharide (LPS) and 300ng/ml Brefeldin A for 16 hours (Image A); No staining on untreated TU-87 MG cell pellets (Image B).
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-6 antibody [RM1304] (AB324449)
Immunohistochemical analysis of paraffin-embedded Image A THP-1 (human monocytic leukemia monocyte) cell pellets treated with 80nM Phorbol-12-myristate-13-acetate (PMA) for 24 hours, then added 100ng/ml Lipopolysaccharides (LPS) for 7 hours, 1µg/ml Brefeldin A was added for additional 3 hours after LPS was added for 4 hours Image B Untreated THP-1 cell pellets tissue labeling IL-6 with ab324449 at 1/200 (2.585 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Cytoplasmic staining on THP-1 (human monocytic leukemia monocyte) cell pellets treated with 80nM Phorbol-12-myristate-13-acetate (PMA) for 24 hours, then added 100ng/ml Lipopolysaccharides (LPS) for 7 hours, 1µg/ml Brefeldin A was added for additional 3 hours after LPS was added for 4 hours (Image A); No staining on untreated THP-1 cell pellets (Image B).
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-6 antibody [RM1304] (AB324449)
Immunohistochemical analysis of paraffin-embedded Image A Mouse lung treated with 1 ug/ml Lipopolysaccharide (LPS) and 300ng/ml Brefeldin A for 16 hours Image B Untreated mouse lung tissue labeling IL-6 with ab324449 at 1/200 (2.585 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Cytoplasmic staining on Mouse lung treated with 1 ug/ml Lipopolysaccharide (LPS) and 300ng/ml Brefeldin A for 16 hours (Image A); No staining on Untreated mouse lung (Image B).
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-6 antibody [RM1304] (AB324449)
Immunohistochemical analysis of paraffin-embedded Image A RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) cell pellets treated with 100ng/ml Lipopolysaccharide (LPS) for 7 hours, then 1µg/ml Brefeldin A was added for additional 3 hours after LPS was added for 4 hours Image B Untreated RAW 264.7 cell pellets tissue labeling IL-6 with ab324449 at 1/200 (2.585 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Cytoplasmic staining on RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) cell pellets treated with 100ng/ml Lipopolysaccharide (LPS) for 7 hours, then 1µg/ml Brefeldin A was added for additional 3 hours after LPS was added for 4 hours (Image A); No staining on Untreated RAW 264.7 cell pellets (Image B).
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- WB
Supplier Data
Western blot - Anti-IL-6 antibody [RM1304] (AB324449)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression molecular weight observed is consistent with what has been described in the literature (PMID : 12091245 and PMID : 14970177).
The expression of IL-6 is upregulated/downregulated in response to LPS and BFA treatment (PMID : 25838003).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-IL-6 antibody [RM1304] (ab324449) at 1/1000 dilution
Lane 1:
Untreated HUVEC (human umbilical vein endothelial cell), whole cell lysate at 20 µg
Lane 2:
HUVEC treated with 0.5 ug/ml LPS for 4 hours, 300ng/ml BFA then added for additional 20 hours, whole cell lysate at 20 µg
Lane 3:
Untreated U-87 MG (human glioblastoma-astrocytoma epithelial cell), whole cell lysate at 20 µg
Lane 4:
U-87 MG treated with 1 ug/ml LPS and 300ng/ml BFA for 16 hours, whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 17-26 kDa,36 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-IL-6 antibody [RM1304] (AB324449)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-IL-6 antibody [RM1304] (ab324449) at 1/1000 dilution
Lane 1:
Untreated mouse lung tissue lysate at 40 µg
Lane 2:
mouse lung treated with 0.5 ug/ml LPS for 4 hours, 300ng/ml BFA then added for additional 20 hours, tissue lysate at 40 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 23 kDa,36 kDa
false
Exposure time: 180s
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are recombinant multiclonals?
Recombinant multiclonals are a mixture of recombinant antibodies co-expressed from a library of heavy and light chains. They offer several advantages including:
- - The sensitivity of polyclonal antibodies by recognising multiple epitopes
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
View our range of recombinant multiclonal antibodies.
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