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>   home   >   Products   >   Primary Antibodies   >   Signal Transduction   >   Anti-HSPB8/Hsp22 Antibody Picoband™ (monoclonal, 7D8)   

Anti-HSPB8/Hsp22 Antibody Picoband™ (monoclonal, 7D8)

     
  •  - Anti-HSPB8/Hsp22 Antibody Picoband™ (monoclonal, 7D8) ABO14941
    Figure 1. Western blot analysis of HSPB8/Hsp22 using anti-HSPB8/Hsp22 antibody (M02492-2).
    Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions.
    Lane 1: human Hela whole cell lysates;
    Lane 2: human T-47D whole cell lysates;
    Lane 3: rat RH35 whole cell lysates.
    After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with mouse anti-HSPB8/Hsp22 antigen affinity purified monoclonal antibody (Catalog # M02492-2) at 0.5 µg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-mouse IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001) with Tanon 5200 system. A specific band was detected for HSPB8/Hsp22 at approximately 22KD. The expected band size for HSPB8/Hsp22 is at 22KD.
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  •  - Anti-HSPB8/Hsp22 Antibody Picoband™ (monoclonal, 7D8) ABO14941
    Figure 2. Flow Cytometry analysis of CACO-2 cells using anti-HSPB8/Hsp22 antibody (M02492-2).
    Overlay histogram showing CACO-2 cells stained with M02492-2 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with mouse anti-HSPB8/Hsp22 Antibody (M02492-2, 1 µg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-mouse IgG (BA1126, 5-10 µg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was mouse IgG (1 µg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
    detail
  •  - Anti-HSPB8/Hsp22 Antibody Picoband™ (monoclonal, 7D8) ABO14941
    Figure 3. Flow Cytometry analysis of U20S cells using anti-HSPB8/Hsp22 antibody (M02492-2).
    Overlay histogram showing U20S cells stained with M02492-2 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with mouse anti-HSPB8/Hsp22 Antibody (M02492-2, 1 µg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-mouse IgG (BA1126, 5-10 µg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was mouse IgG (1 µg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
    detail
  •  - Anti-HSPB8/Hsp22 Antibody Picoband™ (monoclonal, 7D8) ABO14941
    Figure 4. IF analysis of HSPB8/Hsp22 using anti-HSPB8/Hsp22 antibody (M02492-2).
    HSPB8/Hsp22 was detected in immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 µg/mL mouse anti-HSPB8/Hsp22 Antibody (M02492-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
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Product Information
Application
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • E=ELISA
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immuno electron microscopy
  • EIA=Enzyme Immunoassay
WB, IF, ICC, FC
Primary Accession Q9UJY1
Host Mouse
Isotype Mouse IgG2b
Reactivity Rat, Human
Clonality Monoclonal
Format Lyophilized
Description Anti-HSPB8/Hsp22 Antibody Picoband™ (monoclonal, 7D8) . Tested in Flow Cytometry, IF, ICC, WB applications. This antibody reacts with Human, Rat.
Reconstitution Add 0.2ml of distilled water will yield a concentration of 500ug/ml.
Additional Information
Gene ID 26353
Other Names Heat shock protein beta-8, HspB8, Alpha-crystallin C chain, E2-induced gene 1 protein, Heat shock protein family B member 8, Protein kinase H11, Small stress protein-like protein HSP22, HSPB8, CRYAC, E2IG1, HSP22
Calculated MW 22 kDa
Application Details Western blot, 0.1-0.5 µg/ml, Human, Rat
Immunocytochemistry/Immunofluorescence, 5 µg/ml, Human
Flow Cytometry, 1-3 µg/1x10^6 cells, Human
Subcellular Localization Nucleus. Cytoplasm.
Tissue Specificity Predominantly expressed in skeletal muscle and heart.
Contents Each vial contains 4mg Trehalose, 0.9mg NaCl, 0.2mg Na2HPO4, 0.05mg NaN3.
Clone Names Clone: 7D8
Immunogen E.coli-derived human HSPB8/Hsp22 recombinant protein (Position: M1-T196). Human HSPB8/Hsp22 shares 94.4% and 95.4% amino acid (aa) sequence identity with mouse and rat HSPB8/Hsp22, respectively.
Purification Immunogen affinity purified.
Cross Reactivity No cross-reactivity with other proteins.
Storage Store at -20˚C for one year from date of receipt. After reconstitution, at 4˚C for one month. It can also be aliquotted and stored frozen at -20˚C for six months. Avoid repeated freeze-thaw cycles.
Protein Information
Name HSPB8
Synonyms CRYAC, E2IG1, HSP22
Function Displays temperature-dependent chaperone activity.
Cellular Location Cytoplasm. Nucleus Note=Translocates to nuclear foci during heat shock
Tissue Location Predominantly expressed in skeletal muscle and heart.
Research Areas
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Background

Heat shock protein beta-8 is a protein that in humans is encoded by the HSPB8 gene. The protein encoded by this gene belongs to the superfamily of small heat-shock proteins containing a conservative alpha-crystallin domain at the C-terminal part of the molecule. The expression of this gene in induced by estrogen in estrogen receptor-positive breast cancer cells, and this protein also functions as a chaperone in association with Bag3, a stimulator of macroautophagy. Thus, this gene appears to be involved in regulation of cell proliferation, apoptosis, and carcinogenesis, and mutations in this gene have been associated with different neuromuscular diseases, including Charcot-Marie-Tooth disease.

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$ 370.00
Cat# ABO14941
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