概述

  • 产品名称
    Anti-Calnexin抗体
    参阅全部 Calnexin 一抗
  • 描述
    兔多克隆抗体to Calnexin
  • 特异性
    Recognizes ER membrane, mitochondria and cis-Golgi
  • 经测试应用
    适用于: WB, ICC/IF, IHC-P, IP, IHC-Frmore details
  • 种属反应性
    与反应: Mouse, Rat, Human, Common marmoset
    预测可用于: Dog
  • 免疫原

    Synthetic peptide conjugated to KLH derived from within residues 550 to the C-terminus of Human Calnexin.

    (Peptide available as ab23379.)

  • 阳性对照
    • WB: HeLa, MCF-7, NIH 3T3, MEF1 and PC12 whole cell lysates, mouse brain, liver, heart, kidney, pancreas, testis, skeletal muscle, spinal cord and ovary and rat brain, liver, heart and kidney tissue lysates. ICC/IF: HeLa and wildtype HAP1 cells.

性能

  • 形式
    Liquid
  • 存放说明
    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle. Store In the Dark.
  • 存储溶液
    Preservative: 0.02% Sodium Azide
    Constituents: 1% BSA, PBS, pH 7.4
  • Concentration information loading...
  • 纯度
    Immunogen affinity purified
  • 克隆
    多克隆
  • 同种型
    IgG
  • 研究领域

应用

Our Abpromise guarantee covers the use of ab22595 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

应用 Ab评论 说明
WB Use a concentration of 1 µg/ml. Detects a band of approximately 75 kDa (predicted molecular weight: 90 kDa).
ICC/IF Use a concentration of 1 µg/ml.
IHC-P Use at an assay dependent concentration.
IP Use at an assay dependent concentration.
IHC-Fr Use at an assay dependent concentration.

靶标

图片



  • Predicted band size : 90 kDa
    Observed band size : 80 kDa (why is the actual band size different from the predicted?)

    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 1/10000 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 1/10000 dilution for 1 hour at room temperature before imaging.

  • ab22595 staining Calnexin in wild-type HAP1 cells (top panel) and CANX knockout HAP1 cells (bottom panel). The cells were fixed with 4% formaldehyde (10min), 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 1h. The cells were then incubated with ab22595 at 1μg/ml and ab195889 at 1/250 dilution (shown in pseudocolour red) overnight at +4°C, followed by a further incubation at room temperature for 1h with a goat secondary antibody to Rabbit IgG (Alexa Fluor® 488) (ab150081) at 2 μg/ml (shown in green). Nuclear DNA was labelled in blue with DAPI.

    Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

  • ab22595 staining Calnexin in HeLa cells. The cells were fixed with 100% methanol (5min), 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 1h. The cells were then incubated with ab22595 at 1μg/ml and ab7291 at 1μg/ml overnight at +4°C, followed by a further incubation at room temperature for 1h 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 labelled in blue with DAPI.

    Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).



  • Predicted band size : 90 kDa

    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 : Anti-Calnexin antibody (ab22595) at 1/250 dilution

    Lane 1 : NIH 3T3 whole cell lysate (ab7179)
    Lane 2 : MEF1 (Mouse embryonic fibroblast cell line) Whole Cell Lysate (ab46770)
    Lane 3 : Brain (Mouse) Tissue Lysate (ab27253)
    Lane 4 : Liver (Mouse) Tissue Lysate (ab7935)
    Lane 5 : Heart (Mouse) Tissue Lysate (ab27255)
    Lane 6 : Kidney (Mouse) Tissue Lysate (ab27254)
    Lane 7 : Mouse pancreas tissue lysate - total protein (ab29363)
    Lane 8 : Testis (Mouse) Tissue Lysate - normal tissue (ab4027)
    Lane 9 : Mouse skeletal muscle tissue lysate - total protein (ab29711)
    Lane 10 : Spinal Cord (Mouse) Tissue Lysate (ab50253)
    Lane 11 : Ovary (Mouse) Tissue Lysate (ab35808)
    Lane 12 : PC12 (Rat adrenal pheochromocytoma cell line) Whole Cell Lysate (ab50957)
    Lane 13 : Brain (Rat) Tissue Lysate (ab7942)
    Lane 14 : Liver (Rat) Tissue Lysate (ab27256)
    Lane 15 : Heart (Rat) Tissue Lysate (ab7940)
    Lane 16 : Kidney (Rat) Whole Cell Lysate - normal tissue (ab29480)

    Lysates/proteins at 10 µg per lane.

    Secondary
    IRDye 680 Conjugated Goat Anti-Rabbit IgG (H+L) at 1/10000 dilution

    Performed under reducing conditions.

    Predicted band size : 90 kDa
    Observed band size : 80 kDa (why is the actual band size different from the predicted?)
  • Kidney cortex using ab22595 shows clear cytoplasmic staining patterns. The visceral cells of the Glomerular tuft ( podocytes ) are strongly stained (indicated by red arrowheads). Distal convoluted tubular cells are generally moderately positive (with exceptions that are strongly positive). However, most of the cells that line the Proximal Convoluted Tubules (indicated by green arrowheads) are strongly positive.

    See Abreview

  • All lanes : Anti-Calnexin antibody (ab22595) at 1 µg/ml

    Lane 1 : HeLa (Human epithelial carcinoma cell line)
    Lane 2 : U2OS Whole Cell Lysate
    Lane 3 : MCF-7 (Human breast adenocarcinoma cell line) Whole Cell Lysate
    Lane 4 : HeLa (Human epithelial carcinoma cell line) with Human Calnexin - ER membrane marker peptide (ab23379) at 1 µg/ml
    Lane 5 : U2OS Whole Cell Lysate with Human Calnexin - ER membrane marker peptide (ab23379) at 1 µg/ml
    Lane 6 : MCF-7 (Human breast adenocarcinoma cell line) Whole Cell Lysate with Human Calnexin - ER membrane marker peptide (ab23379) at 1 µg/ml

    Lysates/proteins at 20 µg per lane.

    Secondary
    Goat polyclonal to Rabbit IgG (Alexa Fluor® 680) at 1/10000 dilution

    Performed under reducing conditions.

    Predicted band size : 90 kDa
    Observed band size : 75 kDa (why is the actual band size different from the predicted?)

    Recent batches of ab22595 (AP217379 and AP151845) detect a band of ~ 75 kDa in Hela, U2OS and MCF-7 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.

  • Calnexin - ER membrane marker was immunoprecipitated using 0.5mg Hela whole cell extract, 5µg of Rabbit polyclonal to Calnexin - ER membrane marker and 50µl of protein G magnetic beads (+). No antibody was added to the control (-).
    The antibody was incubated under agitation with Protein G beads for 10min, Hela whole cell extract lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation.
    Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl 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.

文献

This product has been referenced in:
  • Qiu J  et al. A unique deubiquitinase that deconjugates phosphoribosyl-linked protein ubiquitination. Cell Res 27:865-881 (2017). WB . Read more (PubMed: 28497808) »
  • Yang Y  et al. Secretory carrier membrane protein 5 is an autophagy inhibitor that promotes the secretion of a-synuclein via exosome. PLoS One 12:e0180892 (2017). WB ; Rat, Human . Read more (PubMed: 28700687) »

See all 68 Publications for this product

客户评价及客户问答

Application
Western blot
Sample
Sheep Cell lysate - other (total protein, mitochondria and ER isolates)
Gel Running Conditions
Reduced Denaturing (10% PAG)
Loading amount
10 µg
Specification
total protein, mitochondria and ER isolates
Blocking step
Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 10% · Temperature: 23°C
Username

Miss. Barbara Makela

Verified customer

提交于 Mar 08 2017

Abcam guarantees this product to work in the species/application used in this Abreview.
Application
Immunocytochemistry/ Immunofluorescence
Sample
Human Cell (HEK 293t, HFF)
Permeabilization
Yes - 0.1% TX-100, 0.01% SDS in 1xPBS
Specification
HEK 293t, HFF
Blocking step
Serum as blocking agent for 20 minute(s) · Concentration: 10% · Temperature: RT°C
Fixative
Formaldehyde
Username

Miss. Kim JEONG-JIN

Verified customer

提交于 Feb 20 2017

Abcam guarantees this product to work in the species/application used in this Abreview.
Application
Immunocytochemistry/ Immunofluorescence
Sample
Human Cell (primary keratinocyte)
Permeabilization
Yes - 0.4% TritonX100
Specification
primary keratinocyte
Blocking step
BSA as blocking agent for 30 minute(s) · Concentration: 12% · Temperature: 25°C
Fixative
Paraformaldehyde
Username

Abcam user community

Verified customer

提交于 Sep 05 2016

Abcam guarantees this product to work in the species/application used in this Abreview.
Application
Immunohistochemistry (Frozen sections)
Sample
Human Tissue sections (face skin)
Permeabilization
Yes - 0.4% TritonX100
Specification
face skin
Blocking step
Serum as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 10% · Temperature: 25°C
Fixative
Acetone
Username

Abcam user community

Verified customer

提交于 Sep 01 2016

Application
Immunocytochemistry
Sample
Rat Cultured Cells (primary Hippocampal neuron)
Permeabilization
Yes - 0.2% Triton X-100 in PBS
Specification
primary Hippocampal neuron
Blocking step
BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 3% · Temperature: 23°C
Fixative
Paraformaldehyde
Username

Abcam user community

Verified customer

提交于 Mar 11 2016

Application
Western blot
Sample
Rat Cell lysate - whole cell (RBL-2H3 cell)
Gel Running Conditions
Reduced Denaturing
Loading amount
10 µg
Specification
RBL-2H3 cell
Blocking step
Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 20°C
Username

Abcam user community

Verified customer

提交于 Sep 11 2015

Application
Western blot
Sample
Human Cell lysate - whole cell (HEK293T cells)
Gel Running Conditions
Reduced Denaturing
Loading amount
10 µg
Specification
HEK293T cells
Blocking step
Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 20°C
Username

Abcam user community

Verified customer

提交于 Jun 19 2015

Application
Western blot
Loading amount
10000 cells
Gel Running Conditions
Reduced Denaturing (4-12% gradient)
Sample
Human Cell lysate - whole cell (Huh7 liver)
Specification
Huh7 liver
Blocking step
Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
Username

Abcam user community

Verified customer

提交于 Feb 05 2015

Application
Western blot
Loading amount
10 µg
Gel Running Conditions
Reduced Denaturing (16%)
Sample
Mouse Cell lysate - whole cell (Primary bone marrow derived macrophage)
Specification
Primary bone marrow derived macrophage
Blocking step
Milk as blocking agent for 30 minute(s) · Concentration: 5% · Temperature: 20°C
Username

Abcam user community

Verified customer

提交于 Oct 16 2014

Application
Immunocytochemistry/ Immunofluorescence
Blocking step
Serum as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 3% · Temperature: 25°C
Sample
Human Cell (ovarian)
Specification
ovarian
Permeabilization
Yes - 0.1% triton X for 5 min at RT
Fixative
Paraformaldehyde
Username

Abcam user community

Verified customer

提交于 Aug 25 2014

1-10 of 32 Abreviews or Q&A

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

注册