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Recombinant Human Sorting nexin-14 (SNX14), partial

CAT: 0013-GTR19127128-01Size: 20 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR19127128-01Size:20 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
This Recombinant Human Sorting nexin-14 (SNX14), partial spans the amino acid sequence from region 130-304. Purity: Greater than 85% as determined by SDS-PAGE.
Product Name Alternative
Sorting nexin-14 SNX14
UniProt
Q9Y5W7
Expression Region
130-304
Origin
Homo sapiens (Human)
Field of Research
Neuroscience
Endotoxin
Not test
Purity
Greater than 85% as determined by SDS-PAGE.
Form
Liquid or Lyophilized powder
Storage Conditions
Storage: The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself. Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C. Notes: Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week
Notes
For research use only.
Preservative
If the delivery form is liquid, the default storage buffer is Tris/PBS-based buffer, 20%-50% glycerol. If the delivery form is lyophilized powder, the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose.
AA Sequence
SSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSP

UniProtKB · Q9Y5W7

Sorting nexin-14

SNX14_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9Y5W7
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
SNX14
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
B4DI55, Q4VBR3, Q5TCF9, Q5TCG0, Q6NUI7, Q6PI37, Q9BSD1
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Cellular component

Cell projectionEndosomeLysosomeMembrane

Disease

Disease variantIntellectual disabilityNeurodegenerationSpinocerebellar ataxia

PTM

Phosphoprotein

Biological process

Protein transportTransport

Domain

TransmembraneTransmembrane helix

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