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Human BIRC7 / Livin Recombinant Protein - LS-G44870

Catalog Size Price
LS-G44870-5 5 µg Unavailable

Most Popular BIRC7 / Livin Proteins

Human BIRC7 / Livin Recombinant (His) Protein - LS-G1639
E. coli Expression System
304 AA
His
Purified
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image
Human BIRC7 / Livin Recombinant (His) Protein - LS-G3489
E. coli Expression System
318 AA
His
Purified
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image
Human BIRC7 / Livin Recombinant (His) Protein - LS-G18691
E. coli Expression System
His
Purified
Human BIRC7 / Livin Recombinant (His) Protein - LS-G20010
E. coli Expression System
His
Purified
Human BIRC7 / Livin Recombinant (GST) Protein - LS-G35196
Wheat Wheat Germ Extract
298 AA
GST
Purified
Sodium Dodecyl Sulfate - Polyacrylamide Gel Electrophoresis Image

100% Guaranteed
LS-G44870
Recombinant Protein
BIRC7 / Livin
Human
MGSSHHHHHH SSGLVPRGSH MGPKDSAKCL HRGPQPSHWA
AGDGPTQERC GPRSLGSPVL GLDTCRAWDH VDGQILGQLR
PLTEEEEEEG AGATLSRGPA FPGMGSEELR LASFYDWPLT
AEVPPELLAA AGFFHTGHQD KVRCFFCYGG LQSWKRGDDP
WTEHAKWFPS CQFLLRSKGR DFVHSVQETH SQLLGSWDPW
EEPEDAAPVA PSVPASGYPE LPTPRREVQS ESA
E. coli
E. coli
None
Greater than 90% by SDS-PAGE and RP-HPLC
Not Tested
Not Tested
20 mM Tris, pH 8, 1 mM DTT, 0.1 M NaCl, 2 mM EDTA, 20% glycerol
For research use only.

About BIRC7 / Livin

Q96CA5 NM_022161 NP_071444.1

BIRC7 Protein, KIAP Protein, Livin inhibitor of apoptosis Protein, MLIAP Protein, ML-IAP Protein, RNF50 Protein, RING finger protein 50 Protein, LIVIN Protein

Apoptotic regulator capable of exerting proapoptotic and anti-apoptotic activities and plays crucial roles in apoptosis, cell proliferation, and cell cycle control. Its anti-apoptotic activity is mediated through the inhibition of CASP3, CASP7 and CASP9, as well as by its E3 ubiquitin-protein ligase activity. As it is a weak caspase inhibitor, its anti-apoptotic activity is thought to be due to its ability to ubiquitinate DIABLO/SMAC targeting it for degradation thereby promoting cell survival.

Requested From: 
Date Requested: 6/22/2017

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