Recombinant Glutamate Cysteine Ligase, Modifier Subunit (GCLM)
-
Catalog number
RPU52033
-
Price
Please ask
-
Size
10 μg
-
-
Verified reactivity
Homo sapiens (Human)
-
Protein number
P48507
-
Gene name
Please refer to GenBank
-
Other name
GLCLR; GECS; GCL; Gamma Glutamylcysteine Synthetase; Glutamate Cysteine Ligase Regulatory; Gamma-ECS regulatory subunit; Glutamate cysteine ligase modifier subunit
-
Protein origin
E.coli
-
Protein region
Please contact us.
-
Protein sequence
Please contact us.
-
Information about sequence
Ser40~Ser251
-
Expected molecular weight
27,7kDa
-
Protein purity
≥ 95%
-
Verified applications
SDS-PAGE; WB; ELISA; IP.
-
Storage recommendation
Aliquot and store at -20°C. Minimize freezing and thawing.
-
Use before
1 year
-
Shipping requirements
Blue ice
-
Estimated production time
7-11 business days
-
Notes
For research use only. Not for diagnostic procedures.
-
-
Gene
Cys or cysteines ChEMBL54943
-
Source
Recombinants or rec. proteins
-
Group
recombinants
-
Gene target
-
Gene symbol
GCLM
-
Short name
Recombinant Glutamate Cysteine Ligase, Modifier Subunit (GCLM)
-
Technique
Recombinant, E. coli recombinant proteins are genetic recombinations in Escherichia coli, supplied as white sterile powder lyopillized. bioma advises they will be reconstituted in a buffer soluion or culture medium for cell culture.
-
Label
two N-terminal Tags, His-tag and T7-tag
-
Alternative name
Rec. Glutamate Cysteine Ligase, Modifier functionnal sequence (glutamate-cysteine ligase, modifier subunit)
-
Alternative technique
rec
-
Alternative to gene target
glutamate-cysteine ligase, modifier subunit, GLCLR, GCLM and IDBG-100355 and ENSG00000023909 and 2730, protein heterodimerization activity, Cytoplasm, Gclm and IDBG-191550 and ENSMUSG00000028124 and 14630, GCLM and IDBG-636430 and ENSBTAG00000007842 and 525659
-
Gene info
MeSH Data
-
Name
-
Concept
Scope note:
A DNA amplification technique based upon the ligation of OLIGONUCLEOTIDE PROBES. The probes are designed to exactly match two adjacent sequences of a specific target DNA. The chain reaction is repeated in three steps in the presence of excess probe: (1) heat denaturation of double-stranded DNA, (2) annealing of probes to target DNA, and (3) joining of the probes by thermostable DNA ligase. After the reaction is repeated for 20-30 cycles the production of ligated probe is measured.
-
Tree numbers
-
Qualifiers
ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data
Similar products