Solute Carrier Family 22 Member 5 (SLC22A5) (C-Term) Peptide
SLC22A5
Reactivity: Human
Host: Synthetic
BP, WB
Catalog No. ABIN983873
$160.46
Plus shipping costs $50.00
100 μg
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Quick Overview for Solute Carrier Family 22 Member 5 (SLC22A5) (C-Term) Peptide (ABIN983873)
Target
SLC22A5
(Solute Carrier Family 22 Member 5 (SLC22A5))
Origin
Human
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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Protein Region
- C-Term
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Sequence
- GIVVPSTIFD PSELQDLSSK KQQSHNILDL LRTWNIRMVT IMSIMLWMTI
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Characteristics
- This is a synthetic peptide designed for use in combination with anti-SLC22A5 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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Purification
- Purified
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Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Concentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Handling Advice
- Avoid repeated freeze-thaw cycles.
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Storage
- -20 °C
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Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))
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Background
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Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy.
Alias Symbols: CDSP, FLJ46769, OCTN2, OCTN2VT
Protein Interaction Partner: PDZD3,PDZK1,SLC9A3R1,SLC9A3R2
Protein Size: 557 -
Molecular Weight
- 61 kDa
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Gene ID
- 6584
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NCBI Accession
- NM_003060, NP_003051
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UniProt
- O76082
Target
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