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

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DCTN1 단백질을 인식하는 Thermo Fisher Scientific의 Sheep Polyclonal Antibody로, WB와 IHC에 사용 가능. 인간, 생쥐, 랫드 반응성. 합성 펩타이드 항원 기반, Lyophilized 형태로 제공되며 보존제가 없음. 연구용으로만 사용.

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마지막 업데이트 2025. 07. 23. 오전 06:47
Thermo Fisher Scientific OSD00018W-100UL DCTN1 Polyclonal Antibody 100 ul pk판매 단위 pk
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563,100원VAT 포함 619,410원

Thermo Fisher Scientific · Thermo Fisher Scientific DCTN1 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:300–1:2,000

Immunohistochemistry (IHC)

  • Tested Dilution: 1:300–1:2,000

Miscellaneous PubMed (Misc)

  • View 3 publications

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Sheep / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from aa region 120–170 of human DCTN1 conjugated to an immunogenic carrier protein
Conjugate Unconjugated
Form Lyophilized
Concentration Not Determined
Storage Buffer Whole serum
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 added stability.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Reconstitute in 100 µL of sterile water. Centrifuge to remove any insoluble material.
  • The peptide is homologous in rat and mouse.
  • Specificity: DCTN1.

Target Information

This gene encodes the largest subunit of dynactin, a macromolecular complex consisting of 10 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. It is involved in various cellular functions such as ER-to-Golgi transport, lysosome and endosome movement, spindle formation, chromosome movement, nuclear positioning, and axonogenesis.
This subunit interacts with dynein intermediate chain and binds to microtubules via a conserved CAP-Gly domain in its N-terminus.
Alternative splicing results in multiple transcript variants encoding distinct isoforms.
Mutations in this gene 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. Not for resale without express authorization.

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