Caspr2 (CNTNAP2) (NM_014141) Human Mass Spec Standard

CAT#: PH310836

CNTNAP2 MS Standard C13 and N15-labeled recombinant protein (NP_054860)



  View other "Caspr2" proteins (3)

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CNY 19,520.00


货期*
4周

规格
    • 10 ug

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经常一起买 (2)
Transient overexpression lysate of contactin associated protein-like 2 (CNTNAP2)
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Mouse monoclonal CASPR2 Antibody
    • 100 ug

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Specifications

Product Data
Description CNTNAP2 MS Standard C13 and N15-labeled recombinant protein (NP_054860)
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC210836
Predicted MW 148.2 kDa
Protein Sequence
Tag C-Myc/DDK
Purity > 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration >0.05 µg/µL as determined by microplate BCA method
Labeling Method Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine
Buffer 25 mM Tris-HCl, 100 mM glycine, pH 7.3
Reference Data
RefSeq NP_054860
RefSeq Size 9894
RefSeq ORF 3993
Synonyms AUTS15; CASPR2; CDFE; NRXN4; PTHSL1
Locus ID 26047
Cytogenetics 7q35-q36.1
Summary 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]
Protein Families Druggable Genome, Transmembrane
Protein Pathways Cell adhesion molecules (CAMs)
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