THNSL2 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5142996-Each-of-1 | In Stock | ₹ 40,317.00 |
PIPA5142996 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 40,317.00
GST (18%): ₹ 7,257.06
Total Price: ₹ 47,574.06
Antigen
THNSL2
Classification
Polyclonal
Conjugate
Unconjugated
Gene
THNSL2
Gene Alias
BC051244; FLJ10916; FLJ35504; RGD1309144; secreted osteoclastogenic factor of activated T cells; Secreted osteoclastogenic factor of activated T-cells; SOFAT; THNSL2; threonine synthase like 2; threonine synthase-like 2; threonine synthase-like 2 (bacterial); threonine synthase-like 2 (S. cerevisiae); THS2; TSH2
Host Species
Goat
Purification Method
Ammonium sulfate precipitation
Regulatory Status
RUO
Gene ID (Entrez)
55258
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Isotype
IgG
Applications
Immunohistochemistry (Paraffin), Western Blot
Concentration
0.5 mg/mL
Formulation
TBS with 0.5% BSA and 0.02% sodium azide; pH 7.3
Gene Accession No.
Q86YJ6
Gene Symbols
THNSL2
Immunogen
Peptide with sequence C-SRFRHREVVHLSR.
Quantity
100 μg
Primary or Secondary
Primary
Target Species
Human
Form
Liquid
Related Products
Description
- Additional Information: This antibody is expected to recognize isoform 1 (NP_060741.3) and isoform 2 (NP_001231605.1) only
- This antibody is tested in Peptide ELISA: antibody detection limit dilution 1:128,000
- THNSL2 (threonine synthase-like 2), also known as TSH2, is a 484 amino acid protein belonging to the threonine synthase family
- Utilizing pyridoxal phosphate as a cofactor, THNSL2 may function as a catabolic phospholyase on gamma and beta phosphorylated substrates
- THNSL2 may also degrade O-phospho-threonine to alpha-ketobutyrate, ammonia and phosphate
- Existing as four alternatively spliced isoforms, THNSL2 is encoded by a gene mapping to human chromosome 2p11.2
- As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes
- A number of genetic diseases are linked to genes on chromosome 2
- Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene
- The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8 gene defects
- An extremely rare recessive genetic disorder, Alstrom syndrome, is related to mutations in the ALMS1 gene.