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CSTB antibody

The Rabbit Monoclonal anti-CSTB antibody has been validated for WB. It is suitable to detect CSTB in samples from Human.
Catalog No. ABIN7266617

Quick Overview for CSTB antibody (ABIN7266617)

Target

See all CSTB Antibodies
CSTB (Cystatin B (Stefin B) (CSTB))

Reactivity

  • 92
  • 30
  • 24
  • 13
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
Human

Host

  • 101
  • 24
  • 1
  • 1
Rabbit

Clonality

  • 98
  • 28
Monoclonal

Conjugate

  • 65
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  • 9
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CSTB antibody is un-conjugated

Application

  • 86
  • 60
  • 36
  • 34
  • 23
  • 18
  • 13
  • 13
  • 11
  • 10
  • 5
  • 4
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Western Blotting (WB)
  • Purpose

    Cystatin B Rabbit mAb

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of Human Cystatin B.

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    CSTB (Cystatin B (Stefin B) (CSTB))

    Alternative Name

    Cystatin 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). 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.,CSTB,CPI-B,CST6,EPM1,EPM1A,PME,STFB,ULD,Epigenetics & Nuclear Signaling,RNA Binding,Cell Biology & Developmental Biology,Ubiquitin,Cystatin B

    Molecular Weight

    11kDa

    Gene ID

    1476

    UniProt

    P04080

    Pathways

    Response to Water Deprivation
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