SKU: WP11920 Categories: ,

Cystatin B Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP11920-100
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Product details

Background:

The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and kininogens. This gene encodes a stefin that functions as an intracellular thiol protease inhibitor. The protein is able to form a dimer stabilized by noncovalent forces, inhibiting papain and cathepsins l, h and b. The protein is thought to play a role in protecting against the proteases leaking from lysosomes. Evidence indicates that mutations in this gene are responsible for the primary defects in patients with progressive myoclonic epilepsy (EPM1). One type of mutation responsible for EPM1 is the expansion in the promoter region of this gene of a CCCCGCCCCGCG rep

Specifications

Size50μL/100μL
TargetCystatin B
ReactivityHuman, Rat
ApplicationsWB, IHC, IF, ELISA
MW(Calculated)
MW(Observed)11kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-1:2000; IHC 1:100-1:300; IF 1:200-1:1000; ELISA 1:20000; Not yet tested in other applications. / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenThe antiserum was produced against synthesized peptide derived from human Stefin B. AA range:49-98
SpecificityCystatin B Polyclonal Antibody detects endogenous levels of Cystatin B protein.
Gene NameCSTB
Protein NameCystatin-B
Other NameCSTB; / CST6; / STFB; / Cystatin-B; / CPI-B; / Liver thiol proteinase inhibitor; / Stefin-B
SpeciesHuman
Gene ID1476
UniprotP04080,
Species.1Mouse
Gene ID.1
Uniprot.1Q62426,
Species.2Rat
Gene ID.225308
Uniprot.2P01041
Cellular LocalizationCytoplasm . Nucleus .
Tissue ExpressionCerebellum,Placenta,
Signaling_pathway
Research Areas
FunctionDisease:Defects in CSTB are the cause of progressive myoclonic epilepsy type 1 (EPM1) [MIM:254800]. EPM1 is 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.,Function:This is an intracellular thiol proteinase inhibitor. Tightly binding reversible inhibitor of cathepsins L, H and B.,similarity:Belongs to the cystatin family.,subunit:Able to form dimers stabilized by noncovalent forces.,
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