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Recombinant Human Seipin (BSCL2)

CAT: 0013-GTR19100794-01Size: 20 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR19100794-01Size: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 Seipin (BSCL2) spans the amino acid sequence from region 1-398.
Product Name Alternative
Seipin, Bernardinelli-Seip congenital lipodystrophy type 2 protein
UniProt
Q96G97
Expression Region
1-398
Origin
Homo sapiens (Human)
Field of Research
Metabolism Research
Form
Lyophilized powder
Storage Conditions
Storage Condition: Store at -20°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles. Shelf Life: 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
Tris/PBS-based buffer, 6% Trehalose, pH 8.0
AA Sequence
MVNDPPVPALLWAQEVGQVLAGRARRLLLQFGVLFCTILLLLWVSVFLYGSFYYSYMPTV SHLSPVHFYYRTDCDSSTTSLCSFPVANVSLTKGGRDRVLMYGQPYRVTLELELPESPVN QDLGMFLVTISCYTRGGRIISTSSRSVMLHYRSDLLQMLDTLVFSSLLLFGFAEQKQLLE VELYADYRENSYVPTTGAIIEIHSKRIQLYGAYLRIHAHFTGLRYLLYNFPMTCAFIGVA SNFTFLSVIVLFSYMQWVWGGIWPRHRFSLQVNIRKRDNSRKEVQRRISAHQPGPEGQEE STPQSDVTEDGESPEDPSGTEGQLSEEEKPDQQPLSGEEELEPEASDGSGSWEDAALLTE ANLPAPAPASASAPVLETLGSSEPAGGALRQRPTCSSS

UniProtKB · Q96G97

Seipin

BSCL2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q96G97
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
BSCL2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
G3XAE4, Q567S1, Q96SV1, Q9BSQ0
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Disease

Congenital generalized lipodystrophyDiabetes mellitusDisease variantHereditary spastic paraplegiaNeurodegenerationNeuropathy

PTM

Disulfide bondGlycoproteinPhosphoprotein

Cellular component

Endoplasmic reticulumLipid dropletMembrane

Biological process

Lipid degradationLipid metabolism

Domain

TransmembraneTransmembrane helix

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