Skip to product information
1 of 1

Annexin A1 His Tag Protein, Human

Annexin A1 His Tag Protein, Human

Catalog Number: UA106006 Brand: UA BIOSCIENCE
Price:
Regular price $195 USD
Regular price Sale price $195 USD
Size:

For shipping services or bulk orders, you may request a quotation.
Secure checkout with
View full details

Product Details

Product Specification


Species Human
Synonyms Annexin I, Annexin-1, Calpactin II, Calpactin-2, Chromobindin-9
Accession P04083
Amino Acid Sequence

Ala2-Asn346 with C-10*His

Expression System E.coli
Molecular Weight

Theoretical: 40.4kDa Actual: 40kDa

Purity >95% by SDS-PAGE
Endotoxin <1EU/μg
Conjugation Unconjugated
Tag His Tag
Physical Appearance Lyophilized powder
Reconstitution

Reconstitute no more than 1 mg/mL according to the size in deionized water after rapid centrifugation.

Stability & Storage

12 months from date of receipt, -20 to -70 °C as supplied.
6 months, -20 to -70 °C under sterile conditions after reconstitution.
1 week, 2 to 8 °C under sterile conditions after reconstitution.
Please avoid repeated freeze-thaw cycles.

Background

Annexin A1 belongs to the annexin family of Ca2+-dependent phospholipid-binding proteins. Annexin A1 has important opposing properties during innate and adaptive immune responses: it inhibits innate immune cells and promotes T-cell activation. The activation of T cells results in the release of annexin A1 and the expression of its receptor. This pathway seems to fine-tune the strength of TCR signalling. Higher expression of annexin A1 during pathological conditions could increase the strength of TCR signalling through the mitogen-activated protein kinase signalling pathway, thereby causing a state of hyperactivation of T cells. Annexin A1 has also been of interest for use as a potential anticancer drug. Upon induction by modified NSAIDS and other potent anti-inflammatory drugs, annexin A1 inhibits the NF-κB signal transduction pathway, which is exploited by cancerous cells to proliferate and avoid apoptosis. ANXA1 inhibits the activation of NF-κB by binding to the p65 subunit.

Picture

SDS-PAGE

2μg(R: reducing conditions)