SH3PXD2B (NM_001017995) Human Mass Spec Standard

CAT#: PH314270

SH3PXD2B MS Standard C13 and N15-labeled recombinant protein (NP_001017995)

  View other "SH3PXD2B" proteins (3)

USD 3,255.00

3 Weeks*

    • 10 ug

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Frequently bought together (1)
Transient overexpression lysate of SH3 and PX domains 2B (SH3PXD2B)
    • 100 ug

USD 665.00

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Product Data
Tag C-Myc/DDK
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC214270
Predicted MW 101.4 kDa
Protein Sequence
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
Storage Store at -80°C. Avoid repeated freeze-thaw cycles.
Stability Stable for 3 months from receipt of products under proper storage and handling conditions.
Reference Data
RefSeq NP_001017995
RefSeq Size 7777
RefSeq ORF 2733
Synonyms FAD49; FTHS; HOFI; KIAA1295; TKS4; TSK4
Locus ID 285590
UniProt ID A1X283
Cytogenetics 5q35.1
Summary This gene encodes an adapter protein that is characterized by a PX domain and four Src homology 3 domains. The encoded protein is required for podosome formation and is involved in cell adhesion and migration of numerous cell types. Mutations in this gene are the cause of Frank-ter Haar syndrome (FTHS), and also Borrone Dermato-Cardio-Skeletal (BDCS) syndrome. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015]


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