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Thermo Fisher Scientific Dynactin 1 Monoclonal Antibody (6B11)
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Thermo Fisher Scientific Dynactin 1 Monoclonal Antibody (6B11)

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Dynactin 1 단백질을 특이적으로 인식하는 Mouse 모노클로날 항체로, Western blot 및 Immunoprecipitation에 적합. Human 시료 반응성 검증 완료. 항원 친화 크로마토그래피로 고순도 정제. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 05. 오전 09:29
Thermo Fisher Scientific MA518308 Dynactin 1 Monoclonal Antibody (6B11) 100 ul pk판매 단위 pk ·
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738,100원VAT 포함 811,910원

Thermo Fisher Scientific · Thermo Fisher Scientific Dynactin 1 Monoclonal Antibody (6B11)

Applications and Tested Dilutions

Application Tested Dilution Publications
Western Blot (WB) 1:1,000–1:1,750 View 1 publication
Immunoprecipitation (IP) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human
Published Species Human
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone 6B11
Immunogen Synthetic peptide corresponding to the N-terminal of human Dynactin 1
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2539681

Product Specific Information

  • Detects endogenous levels of DCTN1 (Dynactin 1) at ~150 kDa.
  • No cross-reactivity with related proteins.
  • Purity >95% confirmed by SDS-PAGE.

Target Information

The Dynactin 1 gene encodes the largest subunit of the dynactin complex, which consists of 10 subunits ranging from 22 to 150 kDa. Dynactin binds to both microtubules and cytoplasmic dynein and is involved in various cellular processes such as:

  • ER-to-Golgi transport
  • Centripetal movement of lysosomes and endosomes
  • Spindle formation and chromosome movement
  • Nuclear positioning and axonogenesis

This subunit interacts directly with the dynein intermediate chain and binds 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 are associated with 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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