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Anti-CNTNAP2 Rabbit mAb [50C80K29]

Purified Recombinant Rabbit Monoclonal Antibody

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货号 规格 价格
R015656
20µL ¥588.00
50µL ¥1080.00
100µL ¥1780.00

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Anti-CNTNAP2 Rabbit mAb [50C80K29]
Anti-CNTNAP2 Rabbit mAb [50C80K29]
Anti-CNTNAP2 Rabbit mAb [50C80K29]
Product NameAnti-CNTNAP2 Rabbit mAb
DescriptionPurified Recombinant Rabbit Monoclonal Antibody
Application
  • Applications Legend:
  • WB=Western Blotting
  • IHC-P=Immunohistochemistry (Paraffin)
  • IHC-F=Immunohistochemistry (Frozen)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC-P/IF (Tissue-P), ELISA
DilutionWB 1:1,000~1:2,000; IHC-P 1:100~1:200; IF 1:100~1:200
ReactivityMouse, Rat
HostRabbit
ClonalityMonoclonal
Clone No.50C80K29
IsotypeIgG
LabelUnconjugated
ImmunogenA synthesized peptide derived from human CNTP2
FormatAffinity purified monoclonal antibody supplied in PBS with 0.01% sodium azide and 50% glycerol, pH 7.3.
SynonymsAUTS15; CDFE; Cell recognition molecule Caspr2; CNTNAP2; CNTP2; CNTP2_HUMAN; Contactin-associated protein-like 2; Homolog of Drosophila neurexin IV; NRXN4; PTHSL1.
Molecular weightCalculated MW: 148 kDa; Observed MW: 160 kDa
Uniprot ID Q9UHC6
Gene ID 26047
StorageShipped on wet ice. Store at -20℃. Stable for 24 months from date of receipt. Aliquoting is unnecessary for -20℃ storage.
PrecautionsAnti-CNTNAP2 Rabbit mAb [50C80K29] is for research use only and not for use in diagnostic or therapeutic procedures.
Background 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. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin N-terminal-like domains and a putative PDZ binding site. This protein is localized at the juxtaparanodes of myelinated axons, and mediates interactions between neurons and glia during nervous system development and 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 forkhead box protein P2, 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 intellectual disability. [provided by RefSeq, Jul 2017]
Cellular Location Membrane.
Tissue Location Predominantly expressed in nervous system.

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