SLC19A2 antibody (AA 21-120) (Biotin)
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- Target See all SLC19A2 Antibodies
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
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Binding Specificity
- AA 21-120
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Reactivity
- Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This SLC19A2 antibody is conjugated to Biotin
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Application
- ELISA, Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Specificity
- Possible cross-reactivity with SLC19A3 in human samples
- Cross-Reactivity
- Mouse
- Predicted Reactivity
- Human,Rat,Dog,Cow,Pig,Horse,Rabbit
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human SLC19A2
- Isotype
- IgG
- Top Product
- Discover our top product SLC19A2 Primary Antibody
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- Application Notes
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C for 12 months.
- Expiry Date
- 12 months
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- Target
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
- Alternative Name
- SLC19A2 (SLC19A2 Products)
- Synonyms
- SLC19A2 antibody, TC1 antibody, THMD1 antibody, THT1 antibody, THTR1 antibody, TRMA antibody, solute carrier family 19 member 2 antibody, solute carrier family 19 (thiamine transporter), member 2 antibody, Slc19a2 antibody, SLC19A2 antibody, slc19a2 antibody
- Background
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Synonyms: Thiamine transporter 1, S19A2_HUMAN, SLC19A2, Solute carrier family 19 member 2, TC1, Thiamine carrier 1, THT1, ThTr 1, ThTr-1, ThTr1, TRMA.
Background: This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. [provided by RefSeq, Jul 2008]
- Gene ID
- 10560
- UniProt
- O60779
- Pathways
- Dicarboxylic Acid Transport
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