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Thermo Fisher Scientific Caspr2 Recombinant Rabbit Monoclonal Antibody (001)
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Thermo Fisher Scientific Caspr2 Recombinant Rabbit Monoclonal Antibody (001)

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Thermo Fisher Scientific의 Caspr2 Recombinant Rabbit Monoclonal Antibody (Clone 001)는 Mouse CNTNAP2/CASPR2 단백질에 특이적입니다. ELISA에 최적이며, 높은 특이성과 일관된 로트 간 재현성을 제공합니다. 보존제가 없으며, 장기 보관 시 -20°C에서 보관 권장.

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마지막 업데이트 2025. 07. 27. 오후 04:35
Thermo Fisher Scientific MA529190 Caspr2 Recombinant Rabbit Monoclonal Antibody (001) 100 ul pk판매 단위 pk
재고 1개
569,900원VAT 포함 626,890원

Thermo Fisher Scientific · Thermo Fisher Scientific Caspr2 Recombinant Rabbit Monoclonal Antibody (001)

Applications

  • ELISA (ELISA)
    Tested Dilution: 1:5,000–1:10,000

Product Specifications

항목 내용
Species Reactivity Mouse
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone 001
Immunogen Recombinant Mouse CNTNAP2/CASPR2 protein (Met1–Ser1262)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer PBS, pH 7
Contains No preservative
Storage Conditions Store at 4°C short term. For long term, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2785102

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 antibody DNA sequences from immunoreactive rabbits are cloned and screened to select optimal candidates for production.

Advantages:

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

This antibody has specificity for Mouse CNTNAP2/CASPR2.

Target Information

The CNTNAP2/CASPR2 gene encodes a member of the neurexin family, functioning in the vertebrate nervous system as cell adhesion molecules and receptors.
This protein contains epidermal growth factor repeats, laminin G domains, F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin N-terminal-like domains, and a putative PDZ binding site.

It is localized at the juxtaparanodes of myelinated axons and mediates neuron–glia interactions during nervous system development. It also contributes to potassium channel localization in differentiating axons.

This gene accounts for ~1.5% of chromosome 7 and is among the largest genes in the human genome. It is directly regulated by FOXP2, associated with speech and language development.
Mutations or dysregulation have been implicated in neurodevelopmental disorders such as Tourette syndrome, schizophrenia, epilepsy, autism, ADHD, and mental retardation.


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

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