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Cystatin B/Stefin B Antibody (CPTC-CSTB-3) [DyLight 488]

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Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB, IHC
Clone
CPTC-CSTB-3
Clonality
Monoclonal
Host
Mouse
Conjugate
DyLight 488

Order Details

Cystatin B/Stefin B Antibody (CPTC-CSTB-3) [DyLight 488] Summary

Immunogen
Recombinant full-length human Cystatin B/Stefin B protein (Uniprot: P04080)
Localization
Cytoplasm and nucleus
Marker
Marker of Epithelial Ovarian Cancer Progression
Isotype
IgG1 Kappa
Clonality
Monoclonal
Host
Mouse
Gene
CSTB
Purity
Protein A or G purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Immunohistochemistry-Paraffin
  • Western Blot
Application Notes
Optimal dilution of this antibody should be experimentally determined.

Packaging, Storage & Formulations

Storage
Store at 4C in the dark.
Buffer
50mM Sodium Borate
Preservative
0.05% Sodium Azide
Purity
Protein A or G purified

Notes



DyLight (R) is a trademark of Thermo Fisher Scientific Inc. and its subsidiaries.

Alternate Names for Cystatin B/Stefin B Antibody (CPTC-CSTB-3) [DyLight 488]

  • CPI-B
  • CST6cystatin B (liver thiol proteinase inhibitor)10STFBcystatin-B
  • CSTB
  • cystatin B (stefin B)
  • Cystatin B
  • EPM1
  • Liver thiol proteinase inhibitor
  • PME
  • Stefin B
  • stefin-B

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).

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Product General Protocols

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Video Protocols

WB Video Protocol

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Secondary Antibodies

 

Isotype Controls

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Bioinformatics

Gene Symbol CSTB