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Recombinant Human GOLGA2

CAT: 0710-P2400-01Size: 50 µgDry Ice: NoHazardous: No
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CAT#:0710-P2400-01Size:50 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Product Name Alternative
130 kDa cis Golgi matrix protein, 130 kDa cis-Golgi matrix protein, Cis golgi matrix protein GM130, GM130, Gm130 autoantigen, GOGA2_HUMAN, GOLGA 2, Golga2, Golgi autoantigen, Golgi autoantigen golgin subfamily a 2, Golgi matrix protein GM130, Golgin 95
UniProt
Q08379
Expression Region
837-1002
Host
E.Coli
Tag
N-terminal His-IF2DI Tag
Applications
Western Blot, ELISA
Field of Research
Signal Transduction
Purity
Greater than 90% as determined by SDS-PAGE.
Form
Lyophilized powder
Reconstitution
Centrifuge the vial before opening, reconstitute in sterile distilled water to a concentration of 0.1-1 mg/ml by gently pipetting 2-3 times, don't vortex.
Molecular Weight
39.2 kDa
Shipping Conditions
4°C with ice bag
Storage Conditions
The lyophilized protein is stable at -20 °C for up to 1 year. For extended storage, it is recommended to further dilute in working aliquots after reconstitution. The protein solution is stable at ≤ -20 °C for 3 months, or 2-7 days at 2-8 °C under sterile conditions.Avoid repeated freeze/thaw cycle.
Formulation
Lyophilized from a 0.2 μm filtered solution of 10 mM Hepes, 150 mM NaCl with 5% trehalose, pH 7.4.
Organism Species
Human

UniProtKB · Q08379

Golgin subfamily A member 2

GOGA2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q08379
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
GOLGA2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A0A0C4DGS5, Q6GRM9, Q9BRB0, Q9NYF9
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Biological process

Cell cycleCell divisionMitosisProtein transportTransport

Domain

Coiled coil

Cellular component

CytoplasmCytoskeletonGolgi apparatusMembraneMicrotubule

Disease

Disease variantIntellectual disability

PTM

MethylationPhosphoprotein

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