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Thermo Fisher Scientific CNTNAP2 Polyclonal Antibody
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Thermo Fisher Scientific CNTNAP2 Polyclonal Antibody

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CNTNAP2 단백질을 인식하는 Thermo Fisher Scientific의 폴리클로날 항체로, WB 및 IHC에 사용 가능. 인간 시료 반응성. 동결건조 형태로 제공되며, 장기 보관 시 -20°C에서 안정적. 신경 발달 및 관련 질환 연구에 적합.

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마지막 업데이트 2025. 07. 30. 오후 04:07
Thermo Fisher Scientific OSC00192W-100UL CNTNAP2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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563,100원VAT 포함 619,410원

Thermo Fisher Scientific · Thermo Fisher Scientific CNTNAP2 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution Publications
Western Blot (WB) 1:300–1:2,000 -
Immunohistochemistry (IHC) 1:300–1:2,000 -
Miscellaneous PubMed (Misc) - View 3 publications

Product Specifications

항목 내용
Species Reactivity Human
Published Species Not Applicable
Host / Isotype Rabbit / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from extracellular domain of human Contactin associated protein like 2 (CNTNAP2) conjugated to an immunogenic carrier protein was used as the antigen
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.
  • Specificity: CNTNAP2.

Target Information

This gene encodes a member of the neurexin family which functions in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. It includes F5/8 type C, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin N-terminal-like domains, and a putative PDZ binding site.
Localized at the juxtaparanodes of myelinated axons, it mediates interactions between neurons and glia during nervous system development and is involved in localization of potassium channels within differentiating axons.
This gene occupies almost 1.5% of chromosome 7 and is among the largest genes in the human genome. It is directly regulated by FOXP2, a transcription factor related to speech and language development.
Mutations or dysregulation have been implicated in neurodevelopmental disorders such as Gilles de la 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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