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MFSD2A Rabbit Polyclonal Antibody (Fluoro488)

CAT: 0013-GTR18760467Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18760467Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
MFSD2A Rabbit Polyclonal Antibody (Fluoro488)
Product Name Alternative
MFSD2A; MFSD2; NLS1; HMFN0656; PP9177; UNQ300/PRO341; Sodium-dependent lysophosphatidylcholine symporter 1; NLS1; Sodium-dependent LPC symporter 1; Major facilitator superfamily domain-containing protein 2A
UniProt
Q8NA29
Reactivity
Human, Mouse, Rat
Cross Reactivity
No cross-reactivity with other proteins
Immunogen
E.coli-derived human MFSD2A recombinant protein (Position: Q22-L543) . Human MFSD2A shares 81.6% amino acid (aa) sequence identity with mouse MFSD2A.
Target
Sodium-dependent lysophosphatidylcholine symporter 1
Clonality
Polyclonal
Conjugation
Fluoro488
Field of Research
Cell Biology
Purification
Immunogen affinity purified.
Dilution
Optimal dilutions should be determined by end users.
Form
Liquid
Molecular Weight
60 kDa
Storage Conditions
At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
Notes
For research use only.
Applications Notes
Recommended applications are based on the parent unconjugated antibody. Customers may select suitable applications according to their experimental needs.
Host or Source
Rabbit
Preservative
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.
Isotype
Rabbit IgG

UniProtKB · Q8NA29

Sodium-dependent lysophosphatidylcholine symporter 1

NLS1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q8NA29
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
MFSD2A
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
NLS1, Sodium-dependent LPC symporter 1
EC number
—
Processing
—
Secondary accessions
A8K675, Q6UWU5, Q96F59, Q9BRC8
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Cellular component

Cell membraneEndoplasmic reticulumMembrane

Disease

Disease variantPrimary microcephaly

PTM

Disulfide bondGlycoprotein

Biological process

Lipid transportSymportTransport

Domain

TransmembraneTransmembrane helix

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