GAMT Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5119778-Each-of-1 | In Stock | ₹ 44,811.50 |
PIPA5119778 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 44,811.50
GST (18%): ₹ 8,066.07
Total Price: ₹ 52,877.57
Antigen
GAMT
Classification
Polyclonal
Conjugate
Unconjugated
Gene
GAMT
Gene Alias
AA571402; CCDS2; epididymis secretory protein Li 20; GAMT; GMT; guanidinoacetate methyltransferase; guanidinoacetate N-methyltransferase; HEL-S-20; hypothetical protein LOC515270; PIG2; Spintz1; TP53I2; zgc:123136; zgc:123136 protein
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
14431, 25257, 2593
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Immunohistochemistry (Paraffin), Western Blot
Concentration
1 mg/mL
Formulation
TBS with 0.2% BSA, 50% glycerol and 0.05% sodium azide; pH 7.4
Gene Accession No.
O35969, P10868, Q14353
Gene Symbols
GAMT
Immunogen
Recombinant protein within human GAMT aa 1-222
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Positive Control: Hela cell lysate, mouse liver tissue lysate, rat liver tissue lysate, rat kidney tissue, human liver tissue, human placenta tissue
- Subcellular Location: Cytosol,nucleus,cytoplasm
- GAMT is a methyltransferase that converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor
- Defects in its gene have been implicated in neurologic syndromes and muscular hypotonia, probably due to creatine deficiency and accumulation of guanidinoacetate in the brain of affected individuals.The protein encoded by this gene is a methyltransferase that converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor
- Defects in this gene have been implicated in neurologic syndromes and muscular hypotonia, probably due to creatine deficiency and accumulation of guanidinoacetate in the brain of affected individuals
- Two transcript variants encoding different isoforms have been described for this gene.