Anti-Hsp22/HSPB8 antibody [EPR9714] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
- What is this?
Be the first to review this product! Submit a review
|
(1 Publication)
Rabbit Recombinant Monoclonal Hsp22/HSPB8 antibody. Carrier free. Suitable for IHC-P, WB, ICC/IF and reacts with Mouse, Human samples. Cited in 1 publication.
View Alternative Names
CRYAC, E2IG1, HSP22, PP1629, HSPB8, 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
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-Hsp22/HSPB8 antibody [EPR9714] - BSA and Azide free (AB248999)
This data was developed using ab151552, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of A673 cells labeling Hsp22/HSPB8 with ab151552 at 1/50 dilution.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Hsp22/HSPB8 antibody [EPR9714] - BSA and Azide free (AB248999)
This data was developed using ab151552, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded normal Human uterus tissue using ab151552 showing -ve staining.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Hsp22/HSPB8 antibody [EPR9714] - BSA and Azide free (AB248999)
This data was developed using ab151552, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human skeletal muscle tissue labeling Hsp22/HSPB8 with ab151552 at 1/50 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Hsp22/HSPB8 antibody [EPR9714] - BSA and Azide free (AB248999)
This data was developed using ab151552, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded Human Gastric carcinoma tissue using ab151552 showing -ve staining.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Hsp22/HSPB8 antibody [EPR9714] - BSA and Azide free (AB248999)
This data was developed using ab151552, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded Human Cervical carcinoma tissue using ab151552 showing +ve staining.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Hsp22/HSPB8 antibody [EPR9714] - BSA and Azide free (AB248999)
This data was developed using ab151552, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded normal Human brain tissue using ab151552 showing -ve staining.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Hsp22/HSPB8 antibody [EPR9714] - BSA and Azide free (AB248999)
This data was developed using ab151552, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded Mouse brain tissue using ab151552 showing +ve staining.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- WB
Unknown
Western blot - Anti-Hsp22/HSPB8 antibody [EPR9714] - BSA and Azide free (AB248999)
This data was developed using ab151552, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-Hsp22/HSPB8 antibody [EPR9714] (<a href='/en-us/products/primary-antibodies/hsp22-hspb8-antibody-epr9714-ab151552'>ab151552</a>) at 1/1000 dilution
Lane 1:
Fetal heart lysate at 10 µg
Lane 2:
Fetal muscle lysate at 10 µg
Secondary
All lanes:
HRP labeled goat anti-rabbit at 1/2000 dilution
Predicted band size: 21 kDa
false
- WB
Lab
Western blot - Anti-Hsp22/HSPB8 antibody [EPR9714] - BSA and Azide free (AB248999)
This data was developed using the same antibody clone in a different buffer formulation (ab151552).
Lanes 1 - 2 : Merged signal (red and green). Green - ab151552 observed at 212 kDa. Red - loading control ab7291 (Mouse anti-Alpha Tubulin [DM1A]) observed at 55 kDa.
ab151552 was shown to react with Hsp22/HSPB8 in wild-type HeLa cells in Western blot with loss of signal observed in HSPB8 knockout cell line ab265112 (HSPB8 knockout cell lysate ab257468). Wild-type HeLa and HSPB8 knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3 % milk in TBS-T (0.1 % Tween®) before incubation with ab151552 and ab7291 (Mouse anti-Alpha Tubulin [DM1A]) overnight at 4 °C at a 1 in 1000 dilution and a 1 in 20000 dilution respectively. Blots were incubated 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 in 20000 dilution for 1 h at room temperature before imaging.
All lanes:
Western blot - Anti-Hsp22/HSPB8 antibody [EPR9714] (<a href='/en-us/products/primary-antibodies/hsp22-hspb8-antibody-epr9714-ab151552'>ab151552</a>) at 1/1000 dilution
Lane 1:
Wild-type HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 2:
HSPB8 knockout HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 2:
Western blot - Human HSPB8 (Hsp22) knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-hspb8-hsp22-knockout-hela-cell-line-ab265112'>ab265112</a>)
Predicted band size: 21 kDa
Observed band size: 21 kDa
false
Related conjugates and formulations (1)
-
Anti-Hsp22/HSPB8 antibody [EPR9714]
Reactivity data
Product details
ab248999 is the carrier-free version of ab151552.
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 the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Hsp22 plays a critical role in maintaining protein homeostasis as part of a larger chaperone complex. It forms hetero-oligomers with other small heat shock proteins like HSPB1 and HSPB6 enhancing its protein-protective functions. These interactions allow Hsp22 to stabilize cytoskeletal elements and partake in autophagic pathways highlighting its importance during cellular stress conditions.
Pathways
Hsp22 integrates into cellular processes of autophagy and proteostasis. It participates in the chaperone-assisted selective autophagy (CASA) pathway. Here it associates with the cochaperone BAG3 facilitating the degradation of damaged proteins. Hsp22 also plays a role in the heat shock response pathway cooperating with other heat shock proteins like HSP70 to protect cells from damage induced by increased temperatures.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Oncology reports 50: PubMed37732539
2023
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com