Profilin 1 (PFN1) (NM_005022) Human Mass Spec Standard
CAT#: PH302338
PFN1 MS Standard C13 and N15-labeled recombinant protein (NP_005013)
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CNY 19,520.00
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Specifications
Product Data | |
Description | PFN1 MS Standard C13 and N15-labeled recombinant protein (NP_005013) |
Species | Human |
Expression Host | HEK293 |
Expression cDNA Clone or AA Sequence | RC202338 |
Predicted MW | 15.1 kDa |
Protein Sequence |
>RC202338 protein sequence
Red=Cloning site Green=Tags(s) MAGWNAYIDNLMADGTCQDAAIVGYKDSPSVWAAVPGKTFVNITPAEVGVLVGKDRSSFYVNGLTLGGQK CSVIRDSLLQDGEFSMDLRTKSTGGAPTFNVTVTKTDKTLVLLMGKEGVHGGLINKKCYEMASHLRRSQY TRTRPLEQKLISEEDLAANDILDYKDDDDKV |
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_005013 |
RefSeq Size | 1365 |
RefSeq ORF | 420 |
Synonyms | ALS18 |
Locus ID | 5216 |
Cytogenetics | 17p13.2 |
Summary | This gene encodes a member of the profilin family of small actin-binding proteins. The encoded protein plays an important role in actin dynamics by regulating actin polymerization in response to extracellular signals. Deletion of this gene is associated with Miller-Dieker syndrome, and the encoded protein may also play a role in Huntington disease. Multiple pseudogenes of this gene are located on chromosome 1. [provided by RefSeq, Jul 2012] |
Protein Families | Druggable Genome, Stem cell - Pluripotency |
Protein Pathways | Regulation of actin cytoskeleton |
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