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Thermo Fisher Scientific Caspr2 Polyclonal Antibody
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Thermo Fisher Scientific Caspr2 Polyclonal Antibody

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Caspr2 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, Western blot 및 IHC(P) 실험에 적합합니다. Human 시료 반응성이 있으며, 항원 친화 크로마토그래피로 정제되어 높은 특이성과 재현성을 제공합니다.

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마지막 업데이트 2025. 08. 05. 오후 05:53
Thermo Fisher Scientific PA582033 Caspr2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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765,400원VAT 포함 841,940원

Thermo Fisher Scientific · Thermo Fisher Scientific Caspr2 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 0.04–0.4 µg/mL

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:200–1:500

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human CNTNAP2. Recombinant protein control fragment (Product #RP-95158)
Conjugate Unconjugated
Form Liquid
Concentration 0.2 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2789194

Product Specific Information

Immunogen sequence:
CNKDVGAFFE EGMWLRYNFQ APATNARDSS SRVDNAPDQQ NSHPDLAQEE IRFSFSTTKA PCILLYISSF TTDFLAVLVK PTGSLQIRYN LGGTREPYNI DVDHRNMANG QPHSVNITRH EKTIFLKLDH YPSVSYHLPS SS


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 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 interactions between neurons and glia during nervous system development. It is also involved in localization of potassium channels within differentiating axons.
This gene encompasses almost 1.5% of chromosome 7 and is one of the largest genes in the human genome. It is directly bound and regulated by FOXP2, a transcription factor related to speech and language development.
This gene has been implicated in multiple neurodevelopmental disorders, including 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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