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Thermo Fisher Scientific DCTN1 Polyclonal Antibody
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Thermo Fisher Scientific DCTN1 Polyclonal Antibody

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Rabbit polyclonal antibody against human DCTN1 for WB and IHC applications. Recognizes Dynactin 1 protein region 120–170. Suitable for human, mouse, and rat samples. Lyophilized form, reconstituted in sterile water, stored at 4°C or -20°C.

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마지막 업데이트 2025. 08. 04. 오후 10:46
Thermo Fisher Scientific OSD00017G-500UG DCTN1 Polyclonal Antibody 500 ug pk판매 단위 pk ·
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723,400원VAT 포함 795,740원

Thermo Fisher Scientific · Thermo Fisher Scientific DCTN1 Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 10–50 µg/mL -
Immunohistochemistry (IHC) 10–50 µg/mL -
Miscellaneous PubMed (Misc) - View 2 publications

Product Specifications

Property Description
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide from aa region 120–170 of human DCTN1 conjugated to an immunogenic carrier protein
Conjugate Unconjugated
Form Lyophilized
Concentration Not Determined
Purification Ammonium sulfate precipitation
Storage Buffer PBS
Contains No preservative
Storage Conditions Store at 4°C short term. For long-term storage, store at -20°C avoiding freeze/thaw cycles. Glycerol (1:1) may be added for stability.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Reconstitute in 500 µL of sterile water.
  • Centrifuge to remove any insoluble material.
  • The peptide is homologous in rat and mouse.
  • Specificity: DCTN1.

Target Information

The DCTN1 gene encodes the largest subunit of dynactin, a macromolecular complex of 10 subunits (22–150 kDa). Dynactin binds to microtubules and cytoplasmic dynein, participating in:

  • ER-to-Golgi transport
  • Lysosome and endosome movement
  • Spindle formation and chromosome movement
  • Nuclear positioning and axonogenesis

This subunit interacts with dynein intermediate chain and binds microtubules via a conserved CAP-Gly domain at its N-terminus. Alternative splicing produces multiple isoforms. Mutations cause distal hereditary motor neuronopathy type VIIB (HMN7B), also known as distal spinal and bulbar muscular atrophy (dSBMA).

For Research Use Only. Not for use in diagnostic procedures or resale without authorization.

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