SLC16A2 Rabbit Polyclonal Antibody (CAB3636)
- SKU:
- CAB3636
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Signal Transduction
Frequently bought together:
Description
Product Name: | SLC16A2 Rabbit Polyclonal Antibody |
SKU: | CAB3636 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-100 of human SLC16A2 (NP_006508.2). |
Sequence: | MALQ SQAS EEAK GPWQ EADQ EQQE PVGS PEPE SEPE PEPE PEPV PVPP PEPQ PEPQ PLPD PAPL PELE FESE RVHE PEPT PTVE TRGT ARGF QPPE GGFG |
Tested Applications: | WB ELISA |
Recommended Dilution: | WB,1:500 - 1:2000 |
Synonyms: | AHDS; MCT7; MCT8; XPCT; MCT 7; MCT 8; MRX22; DXS128; DXS128E; SLC16A2 |
Positive Sample: | LO2,HT-29,293T,Mouse heart,Mouse kidney,Mouse liver,Rat heart,Rat liver |
Conjugate: | Unconjugated |
Cellular Localization: | Cell membrane, Multi-pass membrane protein. |
Calculated MW: | 60kDa |
Observed MW: | 70kDa |
This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome.
Purification Method: | Affinity purification |
Gene ID: | 6567 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.01% thimerosal,50% glycerol,pH7.3. |