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SAB4200288

Sigma-Aldrich

Anti-Dystrobrevin-β antibody produced in rabbit

enhanced validation

~1.5 mg/mL, affinity isolated antibody

Synonym(s):

Anti-DTNB

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

antigen ~72 kDa

species reactivity

human, rat

enhanced validation

recombinant expression
Learn more about Antibody Enhanced Validation

concentration

~1.5 mg/mL

technique(s)

immunohistochemistry: 20-40 μg/mL using formalin-fixed, paraffin-embedded rat kidney
immunoprecipitation (IP): 15-30 μg using HEK-293T cells overexpressing human dystrobrevin-β
indirect immunofluorescence: 2-4 μg/mL using HEK-293T cells overexpressing human dystrobrevin-β
western blot: 1.5-3.0 μg/mL using lysates of HEK-293T cells overexpressing human dystrobrevin-β

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... DTNB(1838)
rat ... Dtnb(362715)

General description

The Dystrobrevin (DTNB) gene is mapped to human chromosome 2p23.3. β-DB belongs to the dystrobrevin (DB) subfamily of the dystrophin family. β-DB is found only in non-muscle tissues, and is predominantly expressed in the kidney and brain. It is also highly enriched in postsynaptic densities (PSDs). β-DB is a component of the dystrophin-protein complex (DPC).

Specificity

Anti-Dystrobrevin-b specifically recognizes human and rat dystrobrevin-b.

Immunogen

synthetic peptide corresponding to a sequence located near the N-terminus of human dystrobrevin-b (DTNB), conjugated to KLH. The corresponding sequence is identical in human DTNB isoforms 1-5, and highly conserved (single amino acid substitution) in rat and mouse DTNB.

Application

Anti-Dystrobrevin-β antibody produced in rabbit is suitable for:
  • immunoblotting
  • immunofluorescence
  • immunoprecipitation
  • immunohistochemistry

Biochem/physiol Actions

β-Dystrobrevin (β-DB) is essential for the maintenance and organization of DPC-like complexes in non-muscle tissues. In the brain, β-DB interacts with dystrophin in the cortex, hippocampus, and Purkinje cells. It forms complexes with Dp71 for membrane localization and utrophin. β-DB is associated with the neuronal kinesin heavy chains, Kif5A and Kif5B, in the brain. This infers the role β-DB as a motor protein receptor involved in the site-specific cellular transportation of dystrophin-associated protein complex (DPC) components.

Physical form

Solution in 0.01 M phos­phate buffered saline, pH 7.4, containing 15 mM sodium azide.

Storage and Stability

For continuous use, store at 2-8 °C for up to one month. For extended storage, freeze in working aliquots. Repeated freezing and thawing, or storage in “frost-free” freezers,is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilutions should be discarded if not used within 12 hours.

Disclaimer

Unless otherwise stated in our catalog, our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable


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P Macioce et al.
Journal of cell science, 116(Pt 23), 4847-4856 (2003-11-06)
Beta-dystrobrevin, a member of the dystrobrevin protein family, is a dystrophin-related and -associated protein restricted to non-muscle tissues and is highly expressed in kidney, liver and brain. Dystrobrevins are now thought to play an important role in intracellular signal transduction
Derek J Blake et al.
Physiological reviews, 82(2), 291-329 (2002-03-28)
The X-linked muscle-wasting disease Duchenne muscular dystrophy is caused by mutations in the gene encoding dystrophin. There is currently no effective treatment for the disease; however, the complex molecular pathology of this disorder is now being unravelled. Dystrophin is located
Maria Santa Rocca et al.
European journal of medical genetics, 56(1), 62-65 (2012-11-13)
Deletions of the short arm of chromosome 2 are exceedingly rare and only nine cases involving regions from 2p23 to 2pter have been reported to date. Most of these deletions had only been analysed by GTG banding. Here, we report

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