ITGA8 (NM_003638) Human Mass Spec Standard

CAT#: PH318936

ITGA8 MS Standard C13 and N15-labeled recombinant protein (NP_003629)



  View other "ITGA8" proteins (3)

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CNY 19,520.00


货期*
4周

规格
    • 10 ug

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Transient overexpression lysate of integrin, alpha 8 (ITGA8)
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ITGA8 rabbit polyclonal antibody
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Specifications

Product Data
Description ITGA8 MS Standard C13 and N15-labeled recombinant protein (NP_003629)
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC218936
Predicted MW 117.3 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_003629
RefSeq Size 3261
RefSeq ORF 3189
Locus ID 8516
Cytogenetics 10p13
Summary Integrins are heterodimeric transmembrane receptor proteins that mediate numerous cellular processes including cell adhesion, cytoskeletal rearrangement, and activation of cell signaling pathways. Integrins are composed of alpha and beta subunits. This gene encodes the alpha 8 subunit of the heterodimeric integrin alpha8beta1 protein. The encoded protein is a single-pass type 1 membrane protein that contains multiple FG-GAP repeats. This repeat is predicted to fold into a beta propeller structure. This gene regulates the recruitment of mesenchymal cells into epithelial structures, mediates cell-cell interactions, and regulates neurite outgrowth of sensory and motor neurons. The integrin alpha8beta1 protein thus plays an important role in wound-healing and organogenesis. Mutations in this gene have been associated with renal hypodysplasia/aplasia-1 (RHDA1) and with several animal models of chronic kidney disease. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2014]
Protein Families Druggable Genome, Transmembrane
Protein Pathways Arrhythmogenic right ventricular cardiomyopathy (ARVC), Cell adhesion molecules (CAMs), Dilated cardiomyopathy, ECM-receptor interaction, Focal adhesion, Hypertrophic cardiomyopathy (HCM), Regulation of actin cytoskeleton
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