GYS1 Recombinant Rabbit Monoclonal Antibody (SN75-05), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA532308-Each-of-1 | In Stock | ₹ 46,413.50 |
PIMA532308 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,413.50
GST (18%): ₹ 8,354.43
Total Price: ₹ 54,767.93
Antigen
GYS1
Classification
Monoclonal
Concentration
1 mg/mL
Formulation
TBS with 0.05% BSA, 40% Glycerol and 0.05% sodium azide, pH 7.4
Gene Accession No.
A2RRU1, P13807, Q9Z1E4
Gene Symbols
Gys1
Immunogen
Recombinant protein within Human Glycogen synthase aa 638-737
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Applications
Flow Cytometry, Immunocytochemistry, Immunohistochemistry, Western Blot, Western Blot
Clone
SN75-05
Conjugate
Unconjugated
Gene
Gys1
Gene Alias
EC 2.4.1.11, glycogen [starch] synthase, muscle, glycogen synthase, glycogen synthase 1, glycogen synthase 1 (muscle), glycogen synthase 1, muscle, glycogen synthase 3, brain, GSY, GYS, GYS1, Gys3, MGS
Host Species
Rabbit
Purification Method
Protein A
Regulatory Status
RUO
Gene ID (Entrez)
14936, 2997, 690987
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Related Products
Description
- Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems
- The expression systems are developed by cloning in the specific antibody DNA sequences from immunoreactive rabbits
- Then, individual clones are screened to select the best candidates for production
- The advantages of using recombinant rabbit monoclonal antibodies include: better specificity and sensitivity, lot-to-lot consistency, animal origin-free formulations, and broader immunoreactivity to diverse targets due to larger rabbit immune repertoire
- Glycogen Synthase 1 (GYS1) catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1,4-glycoside linkages
- Mutations in this gene are associated with muscle glycogen storage disease
- Alternatively spliced transcript variants encoding different isoforms have been found for this gene.