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Human CDKN2B/p15INK4b Protein, His tag
Human CDKN2B/p15INK4b Protein, His tag
Origin of place Singapore
Model S0A9061-10μg
Supplier ANT BIO PTE.LTD.
Price 100
Hits 0
Updated 8/25/2025
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Product Specification


SpeciesHuman
SynonymsCyclin-dependent kinase 4 inhibitor B, Multiple tumor suppressor 2 (MTS-2), p14-INK4b, p15-INK4b (p15INK4B), MTS2
AccessionP42772
Amino Acid Sequence

Protein sequence (P42772, Met1-Asp138, with C-His tag) MREENKGMPSGGGSDEGLASAAARGLVEKVRQLLEAGADPNGVNRFGRRAIQVMMMGSARVAELLLLHGAEPNCADPATLTRPVHDAAREGFLDTLVVLHRAGARLDVRDAWGRLPVDLAEERGHRDVAGYLRTATGD

Expression SystemE.coli
Molecular WeightPredicted MW: 16.4 kDa Observed MW: 16.4 kDa
Purity>95% by SDS-PAGE
Endotoxin<0.1EU/μg
ConjugationUnconjugated
Tagwith C-His tag
Physical AppearanceLyophilized Powder
Storage BufferLyophilized from a 0.2 μm filtered solution of 0.2M PBS, pH7.4.
ReconstitutionReconstitute no more than 1 mg/mL according to the size in deionized water after rapid centrifugation.
Stability & Storage

12 months from date of receipt, -20 to -70 °C as supplied.
6 months, -20 to -70 °C under sterile conditions after reconstitution.
1 week, 2 to 8 °C under sterile conditions after reconstitution.
Please avoid repeated freeze-thaw cycles.

Background

Cyclin-dependent kinase 4 inhibitor B also known as multiple tumor suppressor 2 (MTS-2) or p15INK4b is a protein that is encoded by the CDKN2B gene in humans. This gene lies adjacent to the tumor suppressor gene CDKN2A in a region that is frequently mutated, deleted, or dysregulated in a wide variety of cancer. This gene encodes a cyclin-dependent kinase inhibitor, also known as p15Ink4b protein, which forms a complex with CDK4 or CDK6, and prevents the activation of the CDK kinases by cyclin D, thus the encoded protein functions as a cell growth regulator that inhibits cell cycle G1 progression. The expression of this gene was found to be dramatically induced by TGF beta, which suggested its role in the TGF beta induced growth inhibition. CDKN2B tumor suppressor gene product p15 has been shown to interact with cyclin-dependent kinase 4.

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