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Invitrogen
SLC6A15 Polyclonal Antibody
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FIGURE: 1 / 1
SLC6A15 Antibody (PA5-87898) in WB
Western blot analysis of SLC6A15 in mouse kidney. Samples were incubated with SLC6A15 Polyclonal antibody (Product # PA5-87898) using a dilution of 1:1,000, followed by HRP Goat Anti-Rabbit IgG (H+L) at a dilution of 1:10,000. Lysates/proteins: 25 µg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 30s.
Product Details
PA5-87898
Product Specifications
Species Reactivity
Mouse
Host/Isotype
Rabbit
/ IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 350-450 of human SLC6A15 (NP_8774991)
Conjugate
Form
Liquid
Concentration
1.74 mg/mL
Purification
Affinity Chromatography
Storage buffer
PBS, pH 7.3, with 50% glycerol
Contains
0.02% sodium azide
Storage conditions
-20°C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2804488
Product Specific Information
Immunogen sequence: LVVFAVLGFK ANVINEKCIT QNSETIMKFL KMGNISQDII PHHINLSTVT AEDYHLVYDI IQKVKEEEFP ALHLNSCKIE EELNKAVQGT GLAFIAFTEA M; Positive Samples: Mouse kidney; Cellular Location: Membrane, Multi-pass membrane protein
Target Information
SLC6A15 (solute carrier family 6 (neutral amino acid transporter), member 15), also known as sodium-dependent neutral amino acid transporter B(0)AT2, transporter v7-3, NTT73 or sodium-coupled branched-chain amino-acid transporter 1 (SBAT1), is a 730 amino acid multi-pass membrane protein that acts as a sodium-dependent neutral amino acid transporter. A member of the sodium neurotransmitter symporter (SNF) family and SLC6A15 subfamily, SLC6A15 differs from other members of its family in that it does not appear to be chloride-dependent. SLC6A15 is expressed in brain and is encoded by a gene that maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4. 5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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Bioinformatics
Protein Aliases: B0AT2 protein; orphan sodium- and chloride-dependent neurotransmitter transporter NTT73; orphan transporter v7-3; Sodium- and chloride-dependent neurotransmitter transporter NTT73; Sodium-dependent neutral amino acid transporter B(0)AT2; Solute carrier family 6 member 15; Transporter v7-3
Gene Aliases: AA536730; AI326450; AI326451; B0at2; Ntt73; Slc6a15; v7-3
UniProt ID: (Mouse) Q8BG16
Entrez Gene ID: (Mouse) 103098
Performance Guarantee
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
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