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Rabbit Polyclonal Anti-Cystatin B antibody (STJ98972)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, ELISA
Recommended dilution: WB 1:500-2000; ELISA 1:10000-20000
Recommended protocols: check protocols
Click or hover above images to see image description for Anti-Cystatin B antibody.
Check alternative names for the antibodyExpand
|CHROW21 antibody|CPI B antibody|CPI-B antibody|CST 6 antibody|CST6 antibody|CSTB antibody|Cystatin B (stefin B) antibody|Cystatin B antibody|Cystatin-B antibody|CYTB antibody|CYTB_HUMAN antibody|EPM1 antibody|EPM1A antibody|Liver thiol proteinase inhibitor antibody|PME antibody|Stefin-B antibody|STF B antibody|STFB antibody|ULD antibody|Anti-Stefin B antibody (ab53725)
SCBT cat No: sc-66854|
Anti-Cystatin B antibody
|Catalogue No.|| |
Anti-Cystatin B antibody detects endogenous Cystatin B .
Synthetic peptide from human protein at AA range: 20-60.
|Recommended dilution|| |
WB 1:500-2000; ELISA 1:10000-20000
Anti-Cystatin B antibody was tube-contained in liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Anti-Cystatin B antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
CHROW21 antibody, CPI B antibody, CPI-B antibody, CST 6 antibody, CST6 antibody, CSTB antibody, Cystatin B (stefin B) antibody, Cystatin B antibody, Cystatin-B antibody, CYTB antibody, CYTB_HUMAN antibody, EPM1 antibody, EPM1A antibody, Liver thiol proteinase inhibitor antibody, PME antibody, Stefin-B antibody, STF B antibody, STFB antibody, ULD antibody
|Database links|| |
|Protein function|| |
This is an intracellular thiol proteinase inhibitor. Tightly binding reversible inhibitor of cathepsins L, H and B.
|Involvement in disease|| |
Epilepsy, progressive myoclonic 1 (EPM1) [MIM:254800]: An autosomal recessive disorder characterized by severe, stimulus-sensitive myoclonus and tonic-clonic seizures. The onset, occurring between 6 and 13 years of age, is characterized by convulsions. Myoclonus begins 1 to 5 years later. The twitchings occur predominantly in the proximal muscles of the extremities and are bilaterally symmetrical, although asynchronous. At first small, they become late in the clinical course so violent that the victim is thrown to the floor. Mental deterioration and eventually dementia develop. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the cystatin family.
|Protein cellular localization|| |
Cytoplasm . Nucleus .
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St John’s Laboratory Ltd.
|Product type|| |
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