Anti-Calnexin 抗体 - ER Marker
Anti-Calnexin antibody - ER Marker
- Lab Essentials
- KO Validated
- 了解详情
5
(28 Reviews)
|
(717 Publications)
Anti-Calnexin antibody - ER Marker (ab22595) is a rabbit polyclonal antibody detecting Calnexin in Western Blot, IP, ICC/IF. Suitable for Human, Mouse, Rat.
- Over 480 publications
- Trusted since 2006
查看别名
Calnexin, IP90, Major histocompatibility complex class I antigen-binding protein p88, p90, CANX
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Calnexin antibody - ER Marker (AB22595)
ab22595 staining Calnexin in HeLa (Human epithelial cell line from cervix adenocarcinoma) cells.
The cells were fixed with 100% methanol for 5 minutes, permeabilized with 0.1% Triton X-100 for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1% PBS-Tween for 1 hour. The cells were then incubated with ab22595 at 1 μg/ml and ab7291 at 1 μg/ml overnight at +4°C, followed by a further incubation at room temperature for 1 hour with a goat secondary antibody to Rabbit IgG (Alexa Fluor® 488) (ab150081) at 2 μg/ml (shown in green) and a goat secondary antibody to Mouse IgG (Alexa Fluor® 594) (ab150120).
Nuclear DNA was labeled in blue with DAPI.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Calnexin antibody - ER Marker (AB22595)
ab22595 staining Calnexin in wild-type HAP1 cells (top panel) and CANX knockout HAP1 cells (bottom panel).
The cells were fixed with 4% formaldehyde for 10 minutes, permeabilized with 0.1% Triton X-100 for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1% PBS-Tween for 1 hour. The cells were then incubated with ab22595 at 1 μg/ml and ab195889 at 1/250 dilution (shown in pseudocolour red) overnight at +4°C, followed by a further incubation at room temperature for 1 hour with a goat secondary antibody to Rabbit IgG (Alexa Fluor® 488) (ab150081) at 2 μg/ml (shown in green).
Nuclear DNA was labeled in blue with DAPI.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- IP
Unknown
Immunoprecipitation - Anti-Calnexin antibody - ER Marker (AB22595)
Calnexin was immunoprecipitated using 0.5 mg HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell extract, 5 μg of Rabbit polyclonal to Calnexin - ER membrane marker and 50 μl of protein G magnetic beads (+).
No antibody was added to the control (-).
The antibody was incubated under agitation with Protein G beads for 10 minutes, HeLa whole cell extract lysate diluted in RIPA buffer was added to each sample and incubated for a further 10 minutes under agitation.
Proteins were eluted by addition of 40 μl SDS loading buffer and incubated for 10 minutes at 70oC; 10 μl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab22595.
Secondary : Goat polyclonal to mouse IgG light chain specific (HRP) at 1/5000 dilution.
Band : 80kDa : Calnexin - ER membrane marker.
All lanes:
Immunoprecipitation - Anti-Calnexin antibody - ER Marker (ab22595)
Predicted band size: 68 kDa
false
- WB
Lab
Western blot - Anti-Calnexin antibody - ER Marker (AB22595)
Lane 1 : Wild-type HAP1 cell lysate (20 μg)
Lane 2 : Calnexin knockout HAP1 cell lysate (20 μg)
Lanes 1 - 2 : Merged signal (red and green). Green - ab22595 observed at 80 kDa. Red - loading control, ab8245, observed at 37 kDa.
This western blot image is a comparison between ab22595 and a competitor's top cited rabbit polyclonal antibody.
All lanes:
Western blot - Anti-Calnexin antibody - ER Marker (ab22595)
Predicted band size: 68 kDa
false
- WB
Lab
Western blot - Anti-Calnexin antibody - ER Marker (AB22595)
Lane 1 : Wild type HAP1 whole cell lysate (20 μg)
Lane 2 : empty lane
Lane 3 : CANX knockout HAP1 whole cell lysate (20 μg)
Lane 4 : empty lane
Lanes 1 - 4 : Merged signal (red and green). Green - ab22595 observed at 80 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab22595 was shown to specifically react with CANX (Calnexin) in wildtype cells as signal was lost in CANX (Calnexin) knockout cells. Wild-type and eCANX (Calnexin) knockout samples were subjected to SDS-PAGE. ab22595 and ab8245 (Mouse anti GAPDH loading control) were incubated overnight at 4°C at 1 dilution and 1/10,000 dilution respectively.
Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed ab216776 secondary antibodies at 1/10,000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-Calnexin antibody - ER Marker (ab22595)
Predicted band size: 68 kDa
Observed band size: 80 kDa
false
- WB
Project1206****
Western blot - Anti-Calnexin antibody - ER Marker (AB22595)
Recent batches of ab22595 (AP217379 and AP151845) detect a band of ~ 75 kDa in HeLa, U-2 OS and MCF7 lysates. This band is completely blocked by the immunizing peptide so we believe this represents Calnexin. Moreoever, a band of the same size is detected by other Calnexin antibodies tested.
All lanes:
Western blot - Anti-Calnexin antibody - ER Marker (ab22595) at 1 µg/mL
Lane 1:
HeLa (Human epithelial carcinoma cell line) whole cell lysate at 20 µg
Lane 2:
U-2 OS (Human bone osteosarcoma epithelial cell line) whole cell lysate at 20 µg
Lane 3:
MCF7 (Human breast adenocarcinoma cell line) whole cell lysate at 20 µg
Lane 4:
HeLa whole cell lysate at 20 µg
Lane 5:
U-2 OS whole cell lysate at 20 µg
Lane 6:
MCF7 whole cell lysate at 20 µg
Secondary
All lanes:
Goat polyclonal to Rabbit IgG (Alexa Fluor® 680) at 1/10000 dilution
Predicted band size: 68 kDa
Observed band size: 75 kDa
false
- WB
PubMed
Western blot - Anti-Calnexin antibody - ER Marker (AB22595)
Subcellular distribution of Smn and hnRNP R in isolated mouse embryonic motoneurons.
Lentiviral knockdown of hnRNP R led to a dose-dependent reduction of hnRNP R levels. Calnexin and Smn protein were not altered significantly.
Primary motoneurons or E18 spinal cord tissue, respectively, were lysed with cytosolic and nuclear fractionation buffer, solubilized in Laemmli buffer and boiled for 10 minutes at 99°C. Proteins were then subjected to SDS-PAGE, blotted onto PVDF membrane, incubated with the corresponding antibodies, including ab22595.
All lanes:
Western blot - Anti-Calnexin antibody - ER Marker (ab22595)
Predicted band size: 68 kDa
false
Dombert et al PLoS One. 2014 Oct 22;9(10):e110846. doi: 10.1371/journal.pone.0110846. eCollection 2014. Fig 1. Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/
- WB
Project
Western blot - Anti-Calnexin antibody - ER Marker (AB22595)
All lanes:
Western blot - Anti-Calnexin antibody - ER Marker (ab22595) at 1/250 dilution
Lane 1:
Western blot - NIH/3T3 whole cell lysate (<a href='/products/cell-lysates/nih-3t3-whole-cell-lysate-ab7179'>ab7179</a>) at 10 µg
Lane 2:
MEF1 (Mouse embryonic fibroblast cell line) Whole Cell Lysate (ab46770) at 10 µg
Lane 3:
Brain (Mouse) Tissue Lysate (ab27253) at 10 µg
Lane 4:
Liver (Mouse) Tissue Lysate (<a href='/products/unavailable/liver-mouse-tissue-lysate-ab7935'>ab7935</a>) at 10 µg
Lane 5:
Heart (Mouse) Tissue Lysate (ab27255) at 10 µg
Lane 6:
Kidney (Mouse) Tissue Lysate (ab27254) at 10 µg
Lane 7:
Western blot - Mouse pancreas tissue lysate - total protein (<a href='/products/tissue-lysates/mouse-pancreas-tissue-lysate-total-protein-ab29363'>ab29363</a>) at 10 µg
Lane 8:
Testis (Mouse) Tissue Lysate - normal tissue (<a href='/products/unavailable/testis-mouse-tissue-lysate-normal-tissue-ab4027'>ab4027</a>) at 10 µg
Lane 9:
Western blot - Mouse skeletal muscle tissue lysate - total protein (<a href='/products/tissue-lysates/mouse-skeletal-muscle-tissue-lysate-total-protein-ab29711'>ab29711</a>) at 10 µg
Lane 10:
Spinal Cord (Mouse) Tissue Lysate (ab50253) at 10 µg
Lane 11:
Ovary (Mouse) Tissue Lysate (ab35808) at 10 µg
Lane 12:
PC-12 (Rat adrenal pheochromocytoma cell line) Whole Cell Lysate (ab50957) at 10 µg
Lane 13:
Brain (Rat) Tissue Lysate (<a href='/products/unavailable/brain-rat-tissue-lysate-ab7942'>ab7942</a>) at 10 µg
Lane 14:
Liver (Rat) Tissue Lysate (ab27256) at 10 µg
Lane 15:
Heart (Rat) Tissue Lysate (<a href='/products/unavailable/heart-rat-tissue-lysate-ab7940'>ab7940</a>) at 10 µg
Lane 16:
Kidney (Rat) Whole Cell Lysate - normal tissue (<a href='/products/unavailable/kidney-rat-whole-cell-lysate-normal-tissue-ab29480'>ab29480</a>) at 10 µg
Secondary
All lanes:
IRDye 680 Conjugated Goat Anti-Rabbit IgG (H+L) at 1/10000 dilution
Predicted band size: 68 kDa
Observed band size: 80 kDa
false
反应性数据
产品详情
Anti-Calnexin antibody - ER Marker (ab22595) is a rabbit polyclonal antibody and is validated for use in ICC/IF, IP, WB in human samples.
Anti-Calnexin antibody - ER Marker (ab22595) has been cited over 482 times in peer reviewed journals, has been used for calnexin staining and is trusted by the scientific community.
Abcam's high quality validation processes ensure Anti-Calnexin antibody - ER Marker (ab22595) has high sensitivity and specificity.
The specificity of Anti-Calnexin antibody - ER Marker (ab22595) has been confirmed by testing in knockout samples.
Anti-Calnexin antibody - ER Marker (ab22595) has 28 independent reviews from customers.
Anti-Calnexin antibody - ER Marker (ab22595) specifically detects Calnexin (UniProt ID: P27824; Molecular weight: 65kDa) and is sold in 100 µg selling sizes.
Calnexin, an endoplasmic reticulum (ER) chaperone protein, plays a crucial role in oncology by influencing the immune response to tumors and cancer cell behavior. It can impair antitumor immunity by inhibiting T-cell infiltration and enhancing PD-1 expression on T cells, which suppresses their activity. Additionally, aberrant O-glycosylation of calnexin is linked to increased cancer cell migration and adhesion.
Explore our range of organelle-specific antibodies and dyes and discover why our reagents are deeply trusted by cell biologists.
性能和储存信息
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分装信息
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Calnexin facilitates the proper folding of newly synthesized proteins by forming a complex with another chaperone protein called ERp57. This interaction helps in creating the correct disulfide bonds in glycoproteins which is essential for their stability and functionality. The complex often referred to as the calnexin cycle is critical in preventing the aggregation and misfolding of proteins within the ER. This process ensures that only correctly folded proteins proceed to the Golgi apparatus for further processing and transport.
Pathways
Calnexin plays an important role in the ER-associated degradation (ERAD) pathway and the unfolded protein response (UPR). In these pathways calnexin ensures that misfolded proteins are retained in the ER or targeted for degradation preventing cellular stress. Calnexin is associated with proteins such as calreticulin another chaperone protein with a similar function in the ER. Together they maintain proteostasis within cells and protect against the accumulation of improperly folded proteins.
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靶点信息
文献 (717)
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