CTH Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA529725-Each-of-1 | In Stock | ₹ 54,468.00 |
PIPA529725 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 54,468.00
GST (18%): ₹ 9,804.24
Total Price: ₹ 64,272.24
Antigen
CTH
Classification
Polyclonal
Conjugate
Unconjugated
Gene
CTH
Gene Alias
0610010I13Rik; AI314617; BC019483; CSE; Cth; cth protein; CTL target antigen; Cys3; cystathionase; cystathionase (cystathionine gamma-lyase); cystathionase isoform 1; cystathionine gamma-lyase; Cystathionine gamma-lyase-like protein; cysteine desulfhydrase; cysteine-protein sulfhydrase; EGK_00877; fb58d08; gamma-cystathionase; H; homoserine deaminase; homoserine dehydratase; LOC102117863; MGC9471; PRB-RA; probasin-related antigen; QccE-22305; synthase; Unknown (protein for MGC:85785); wu:fb48e03; wu:fb58d08; zgc:66001; zgc:85785
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
107869, 1491, 24962
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
1.02 mg/mL
Formulation
PBS with 20% glycerol and 0.025% ProClin 300; pH 7
Gene Accession No.
P18757, P32929, Q8VCN5
Gene Symbols
CTH
Immunogen
Recombinant fragment corresponding to a region within amino acids 194 and 405 of Human CTH
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Recommended positive controls: 293T, A431, HeLa, HepG2, mouse liver, rat liver
- Predicted reactivity: Mouse (84%), Rat (85%), Pig (86%), Bovine (91%)
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- This gene encodes a cytoplasmic enzyme in the trans-sulfuration pathway that converts cystathione derived from methionine into cysteine
- Glutathione synthesis in the liver is dependent upon the availability of cysteine
- Mutations in this gene cause cystathioninuria
- Alternative splicing of this gene results in two transcript variants encoding different isoforms.