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Thermo Fisher Scientific CD171 Recombinant Rabbit Monoclonal Antibody (001)
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Thermo Fisher Scientific CD171 Recombinant Rabbit Monoclonal Antibody (001)

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인간 CD171/L1CAM 단백질을 인식하는 재조합 토끼 단일클론 항체입니다. 높은 특이성과 민감도를 제공하며 로트 간 일관성이 우수합니다. ELISA에 사용 가능하며, 보존제가 없는 액상 형태로 제공됩니다. 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 02. 오후 07:21
Thermo Fisher Scientific MA531004 CD171 Recombinant Rabbit Monoclonal Antibody (001) 100 ul pk판매 단위 pk ·
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3,377,300원VAT 포함 3,715,030원

Thermo Fisher Scientific · Thermo Fisher Scientific CD171 Recombinant Rabbit Monoclonal Antibody (001)

Applications

  • ELISA (ELISA)
    Tested Dilution: 1:250–1:2,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone 001
Immunogen Recombinant Human CD171/L1CAM Protein (Met1–Glu1120)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
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.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2786665

Product Specific Information

This product is preservative-free. It is recommended to add sodium azide to avoid contamination (final concentration 0.05%–0.1%).

Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems. The expression systems are developed by cloning specific antibody DNA sequences from immunoreactive rabbits. Individual clones are screened to select the best candidates for production.

Advantages of recombinant rabbit monoclonal antibodies:

  • Better specificity and sensitivity
  • Lot-to-lot consistency
  • Animal origin-free formulations
  • Broader immunoreactivity due to larger rabbit immune repertoire

This antibody has specificity for Human CD171/L1CAM.

Target Information

L1CAM/CD171 is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting of several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation.

Mutations in the gene cause three X-linked neurological syndromes known by the acronym CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia, and hydrocephalus). Alternative splicing of a neuron-specific exon is thought to be functionally relevant.

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

제품 이미지

  • MA5-31004_CD171_L1CAM_P32004-1_Rabbit.svg
  • MA5-31004_CD171_L1CAM_P32004-1_Rabbit_PDP.jpeg

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