SLC16A2/MCT8 antibody
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- Target See all SLC16A2/MCT8 (SLC16A2) Antibodies
- SLC16A2/MCT8 (SLC16A2) (Solute Carrier Family 16 Member 2 (SLC16A2))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This SLC16A2/MCT8 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Purification
- Affinity purification
- Immunogen
- Recombinant fusion protein of human SLC16A2 (NP_006508.2).
- Isotype
- IgG
- Top Product
- Discover our top product SLC16A2 Primary Antibody
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- Application Notes
- WB 1:500-1:2000
- Restrictions
- For Research Use only
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- Concentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- SLC16A2/MCT8 (SLC16A2) (Solute Carrier Family 16 Member 2 (SLC16A2))
- Alternative Name
- SLC16A2 (SLC16A2 Products)
- Synonyms
- MCT8 antibody, AW105741 antibody, Mct8 antibody, Xpct antibody, AHDS antibody, DXS128 antibody, DXS128E antibody, MCT 7 antibody, MCT 8 antibody, MCT7 antibody, MRX22 antibody, XPCT antibody, solute carrier family 16 member 2 antibody, solute carrier family 16 (monocarboxylic acid transporters), member 2 antibody, SLC16A2 antibody, Slc16a2 antibody
- Background
- SLC16A2,AHDS,DXS128,DXS128E,MCT 7,MCT 8,MCT7,MCT8,MRX22,XPCT,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.
- Molecular Weight
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Observed_MW: 70kDa
Calculated_MW: 59kDa
- Gene ID
- 6567
- UniProt
- P36021
- Pathways
- Hormone Transport
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