SLC29A3 antibody
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- Target See all SLC29A3 Antibodies
- SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This SLC29A3 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Purification
- Affinity purification
- Immunogen
- Recombinant protein of human SLC29A3
- Isotype
- IgG
- Top Product
- Discover our top product SLC29A3 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
- 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
- SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))
- Alternative Name
- SLC29A3 (SLC29A3 Products)
- Synonyms
- ENT3 antibody, HCLAP antibody, HJCD antibody, PHID antibody, Ent3 antibody, 4933435C21Rik antibody, AW987637 antibody, solute carrier family 29 member 3 antibody, solute carrier family 29 (nucleoside transporters), member 3 antibody, SLC29A3 antibody, Slc29a3 antibody
- Background
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Synonyms: ENT3,Equilibrative nucleoside transporter 3,HCLAP,hENT3,HJCD,PHID,S29A3,SLC29A3,Solute carrier family 29 (equilibrative nucleoside transporter) member 3,Solute carrier family 29 (nucleoside transporters) member 3,Solute carrier family 29 member 3
Background: This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.
- Molecular Weight
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Observed_MW: 50kDa
Calculated_MW: 35kDa/51kDa
- Gene ID
- 55315
- UniProt
- Q9BZD2
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