product summary
Loading...
company name :
HUABIO
product type :
antibody
product name :
c-Fos
catalog :
HA751172
quantity :
100μl
price :
649.00 USD
clonality :
monoclonal
host :
domestic rabbit
conjugate :
nonconjugated
clone name :
PSH07-51
reactivity :
human, mouse, rat
application :
western blot, immunoprecipitation, chromatin immunoprecipitation, immunohistochemistry - paraffin section, immunohistochemistry - frozen section
more info or order :
image
image 1 :

Application: IHC-Fr
Species: Mouse
Site: Hypothalamus (restraint stress induced)
Sample: Frozen section
Antibody concentration: 1/4,000
Antigen retrieval: Not required
Important Notice: Blocking buffer and antibody dilution buffer are recommended to use TBS buffer instead of PBS buffer.
image 2 :

Application: IHC-Fr
Species: Mouse
Site: Cerebral cortex (restraint stress induced)
Sample: Frozen section
Antibody concentration: 1/4,000
Antigen retrieval: Not required
Important Notice: Blocking buffer and antibody dilution buffer are recommended to use TBS buffer instead of PBS buffer.
image 3 :

Application: IHC-Fr
Species: Rat
Site: Cerebral cortex (restraint stress induced)
Sample: Frozen section
Antibody concentration: 1/4,000
Antigen retrieval: Not required
Important Notice: Blocking buffer and antibody dilution buffer are recommended to use TBS buffer instead of PBS buffer.
product information
SKU :
HA751172
Target name :
c-Fos
Species reactivity :
Human,Mouse,Rat,Cynomolgus monkey,Pig
Applications :
WB,IHC-Fr,IF-Cell,IHC-P,ChIP,IF-Tissue,IP
Conjugate :
Non-conjugated
Immunogen :
Recombinant protein within human Protein c-Fos aa 1-380.
Uniprot id :
P01100>SwissProt: P01100 Human;SwissProt: P01101 Mouse;SwissProt: P12841 Rat
Host :
Rabbit
Clone number :
PSH07-51
Isotype :
IgG
Size :
100μl
List Price :
649.00 USD
Storage Buffer :
PBS (pH7.4).
Form :
Liquid
Storage Instruction :
Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Purity :
Protein A affinity purified.
Product type :
Recombinant Rabbit monoclonal Antibody
Positive control :
Human brain tissue, mouse brain tissue, mouse hippocampus tissue, HeLa cells serum starved for 40 hours then add 20% FBS for 2 hours, RAW264.7 cells serum starved for 16 hours then add 20% FBS for 4 hours, C6 cells serum starved for 16 hours then add 10% FBS for 30 minutes, HeLa serum starved for 40 hours then add 20% FBS for 2 hours cell lysate, RAW264.7 serum starved for 16 hours then add 200nM PMA for 4 hours cell lysate, C6 serum starved for 16 hours then add 10% FBS for 30 minutes cell lysate.
Molecular wt :
Predicted band size: 41 kDa
Subcellular location :
Nucleus, Endoplasmic reticulum, Cytoplasm, cytosol.
Concentration :
1 mg/mL.
Recommended dilutions :
WB: 1:2,000-1:5,000
;IHC-Fr: 1:4,000-1:10,000
;IF-Cell: 1:1,000-1:2,000
;IHC-P: 1:5,000
;ChIP: Use 0.5~2 μg for 25 μg of chromatin.
;IF-Tissue: 1:4000-1:10,000
;IP: 1-2μg/sample
Pic img4 :
https://storage.huabio.cn/huabio/productImg/HA751172_4.jpg
Pic legend4 :
Western blot analysis of c-Fos on different lysates with Rabbit anti-c-Fos antibody (HA751172) at 1/5,000 dilution.
Lane 1: HeLa cell lysate
Lane 2: HeLa serum starved for 16 hours then add 200 nM TPA for 4 hours cell lysate
Lane 3: RAW264.7 cell lysate
Lane 4: RAW264.7 serum starved for 16 hours then add 200 nM TPA for 4 hours cell lysate
Lysates/proteins at 15 µg/Lane.
Predicted band size: 41 kDa
Observed band size: 41-55 kDa
Exposure time: 10 seconds; ECL: K1801;
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA751172) at 1/5,000 dilution was used in K1803 at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
Pic img5 :
https://storage.huabio.cn/huabio/productImg/HA751172_5.jpg
Pic legend5 :
Immunohistochemical analysis of paraffin-embedded mouse brain (restraint stress induced) tissue with Rabbit anti-c-Fos antibody (HA751172) at 1/5,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA751172) at 1/5,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img6 :
https://storage.huabio.cn/huabio/productImg/HA751172_6.jpg
Pic legend6 :
Immunohistochemical analysis of paraffin-embedded rat brain (restraint stress induced) tissue with Rabbit anti-c-Fos antibody (HA751172) at 1/5,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA751172) at 1/5,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img7 :
https://storage.huabio.cn/huabio/productImg/HA751172_7.jpg
Pic legend7 :
Immunocytochemistry analysis of HeLa cells serum starved for 40 hours then add 20% FBS for 2 hours labeling c-Fos with Rabbit anti-c-Fos antibody (HA751172) at 1/1,000 dilution.
Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-c-Fos antibody (HA751172) at 1/1,000 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
Pic img8 :
https://storage.huabio.cn/huabio/productImg/HA751172_8.jpg
Pic legend8 :
Immunocytochemistry analysis of RAW264.7 cells serum starved for 16 hours then add 20% FBS for 4 hours labeling c-Fos with Rabbit anti-c-Fos antibody (HA751172) at 1/1,000 dilution.
Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-c-Fos antibody (HA751172) at 1/1,000 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
Pic img9 :
https://storage.huabio.cn/huabio/productImg/HA751172_9.jpg
Pic legend9 :
Immunocytochemistry analysis of C6 cells serum starved for 16 hours then add 10% FBS for 30 minutes labeling c-Fos with Rabbit anti-c-Fos antibody (HA751172) at 1/1,000 dilution.
Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-c-Fos antibody (HA751172) at 1/1,000 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
Pic img10 :
https://storage.huabio.cn/huabio/productImg/HA751172_10.jpg
Pic legend10 :
Chromatin immunoprecipitations were performed with cross-linked chromatin from HeLa cells (serum starved for 16 hours and treated with 200 nM TPA for 4 hours) with c-Fos (HA751172) or Normal Rabbit IgG according to the ChIP protocol. The enriched DNA was quantified by real-time PCR using indicated primers. The amount of immunoprecipitated DNA in each sample is represented as signal relative to the total amount of input chromatin, which is equivalent to one.
Pic img11 :
https://storage.huabio.cn/huabio/productImg/HA751172_11.jpg
Pic legend11 :
Application: IF-tissue
Species: Mouse
Site: Cerebral cortex (restraint stress induced)
Sample: Paraffin-embedded section
Antibody concentration: 1/4,000
Important Notice: Blocking buffer and antibody dilution buffer are recommended to use TBS buffer instead of PBS buffer.
Pic img12 :
https://storage.huabio.cn/huabio/productImg/HA751172_12.jpg
Pic legend12 :
c-Fos was immunoprecipitated from 0.2 mg HeLa serum starved for 40 hours then add 20% FBS for 2 hours cell lysate with HA751172 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using HA751172 at 1/2,000 dilution. HRP Conjugated Anti-Rabbit IgG for IP Nano-secondary antibody at 1/5,000 dilution was used for 1 hour at room temperature.
Lane 1: HeLa serum starved for 40 hours then add 20% FBS for 2 hours cell lysate (input)
Lane 2: HA751172 IP in HeLa serum starved for 40 hours then add 20% FBS for 2 hours cell lysate
Lane 3: Rabbit IgG instead of HA751172 in HeLa serum starved for 40 hours then add 20% FBS for 2 hours cell lysate
Blocking/Dilution buffer: primary antibody dilution (K1803)
Exposure time: 59 seconds; ECL: K1801
more info or order :
company information

HUABIO
Founded in 2007, HUABIO is dedicated to developing high-quality antibodies that advance innovation. We are passionate about the accuracy, efficiency, and consistency of our products. That is why we have invested in new production platforms, like recombinant rabbit monoclonals, alpaca nanobodies, and adopted aggressive QA standards to deliver cutting-edge antibodies with uncompromised quality.
We hope to see you at your next discovery!
We hope to see you at your next discovery!
related products
browse more products
questions and comments
