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>   首页   >   产品   >   一抗   >   其他   >   Cystatin B Rabbit mAb   

Cystatin B Rabbit mAb

     
  • 1 - Cystatin B Rabbit mAb AP76461
    Western blot analysis of CystatinB in PC-12 lysates using Cystatin B antibody.
  • 2 - Cystatin B Rabbit mAb AP76461
    Western blot analysis of CystatinB in Hela, A549, HL-60 lysates using CystatinB antibody.
  • 0 - Cystatin B Rabbit mAb AP76461
    Immunohistochemistry analysis of paraffin-embedded Human tonsil using CystatinB antibody. High-pressure and temperature Sodium Citrate pH 6.0 was used for antigen retrieval.
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC-P
Primary Accession P04080
Reactivity Rat, Human
Host Rabbit
Clonality Monoclonal Antibody
Isotype IgG
Conjugate Unconjugated
Purification Affinity Purified
Calculated MW 11140 Da
Additional Information
Gene ID 1476
Other Names CSTB
Dilution WB~~1:1000-1:5000
IHC-P~~1:50~200
Format Liquid in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA.
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Protein Information
Name CSTB
Synonyms CST6, STFB
Function This is an intracellular thiol proteinase inhibitor. Tightly binding reversible inhibitor of cathepsins L, H and B.
Cellular Location Cytoplasm. Nucleus
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

BACKGROUND

Cystatin B (CSTB), a member of the cystatin superfamily protein, is a stefin that functions as an intracellular thiol protease inhibitor and has been thought to play a role in protecting against the proteases leaking from lysosomes. CSTB plays various functions in a variety of diseases, including epithelial ovarian cancer, colon cancer, and myoclonus epilepsy. Evidence indicates that mutations in CSTB 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 repeat from 2-3 copies to 30-78 copies.

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