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Recombinant Human C1QBP

CAT: 0710-P8698-01Size: 50 µgDry Ice: NoHazardous: No
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CAT#:0710-P8698-01Size:50 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Product Name Alternative
C1QBP, gC1Q R, GC1q R protein, GC1QBP, gC1qR, Glycoprotein gC1qBP, HABP1, Hyaluronan binding protein 1, p32, p33, SF2p32
UniProt
Q07021
Expression Region
74-282
Host
E.Coli
Tag
N-terminal His-IF2DI Tag
Applications
Western Blot, ELISA
Field of Research
Immunology, Cardiovascular
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
44.4 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 · Q07021

Complement component 1 Q subcomponent-binding protein, mitochondrial

C1QBP_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q07021
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
C1QBP
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
Precursor
Secondary accessions
Q2HXR8, Q9NNY8
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

PTM

AcetylationPhosphoprotein

Biological process

Adaptive immunityApoptosisComplement pathwayDNA damageHost-virus interactionImmunityInnate immunitymRNA processingmRNA splicingRibosome biogenesisTranscriptionTranscription regulation

Cellular component

Cell membraneCytoplasmMembraneMitochondrionNucleusSecreted

Disease

Disease variantPrimary mitochondrial disease

Domain

Transit peptide

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