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Human GOSR2 protein

CAT: 0013-GTR18882071-01Size: 20 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18882071-01Size:20 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
This Human GOSR2 protein spans the amino acid sequence from region 1-190aa. Purity: Greater than 90% as determined by SDS-PAGE.
Product Name Alternative
GOSR2
UniProt
O14653
Expression Region
1-190aa
Tag
N-terminal 6xHis-SUMO-tagged
Source
E.coli
Origin
Homo sapiens (Human)
Field of Research
Cell Biology
Purity
Greater than 90% as determined by SDS-PAGE.
Form
Liquid or Lyophilized powder
Molecular Weight
38.3 kDa
Storage Conditions
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
For research use only.
Applications Notes
Full length of Cytoplasmic of His-SUMO-tag and expression region is 1-190aa
Preservative
If the delivery form is liquid, the default storage buffer is Tris/PBS-based buffer, 5%-50% glycerol. If the delivery form is lyophilized powder, the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, pH 8.0.
AA Sequence
MDPLFQQTHKQVHEIQSCMGRLETADKQSVHIVENEIQASIDQIFSRLERLEILSSKEPPNKRQNARLRVDQLKYDVQHLQTALRNFQHRRHAREQQERQREELLSRTFTTNDSDTTIPMDESLQFNSSLQKVHNGMDDLILDGHNILDGLRTQRLTLKGTQKKILDIANMLGLSNTVMRLIEKRAFQDK

UniProtKB · O14653

Golgi SNAP receptor complex member 2

GOSR2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O14653
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
GOSR2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
D3DXJ5, D3DXJ6, Q8N4B8, Q96DA5, Q9BZZ4
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

PTM

Acetylation

Coding sequence diversity

Alternative splicing

Domain

Coiled coilTransmembraneTransmembrane helix

Disease

Congenital muscular dystrophyDisease variantEpilepsyNeurodegeneration

Cellular component

Endoplasmic reticulumGolgi apparatusMembrane

Biological process

Protein transportTransport

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