Recombinant Human GC1q R protein (ab172818)
- Datasheet
- References
- Protocols
Overview
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Product nameRecombinant Human GC1q R protein
See all GC1q R proteins and peptides -
Protein lengthFull length protein
Description
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NatureRecombinant
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SourceEscherichia coli
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Amino Acid Sequence
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Accession
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SpeciesHuman
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SequenceMLHTDGDKAFVDFLSDEIKEERKIQKHKTLPKMSGGWELELNGTEAKLVR KVAGEKITVTFNINN SIPPTFDGEEEPSQGQKVEEQEPELTSTPNFVVEVIKNDDGKKALVLDCH YPEDEVGQEDEAESD IFSIREVSFQSTGESEWKDTNYTLNTDSLDWALYDHLMDFLADRGVDNTF ADELVELSTALEHQE YITFLEDLKSFVKSQLEHHHHHH
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Molecular weight31 kDa
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Amino acids74 to 282
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TagsHis tag C-Terminus
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Additional sequence informationMature form.
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Associated products
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Related Products
- Anti-GC1q R antibody (ab101267)
- Anti-GC1q R antibody [74.5.2] (ab125132)
- Anti-GC1q R antibody [60.11] (FITC) (ab125138)
- Anti-6X His tag® antibody [HIS.H8] (ab18184)
- Anti-GC1q R antibody [60.11] (ab24733)
- Anti-GC1q R antibody - Azide free (ab37851)
- Anti-6X His tag® antibody [4D11] (ab5000)
- Anti-6X His tag® antibody - ChIP Grade (ab9108)
Specifications
Our Abpromise guarantee covers the use of ab172818 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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Applications
SDS-PAGE
HPLC
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Endotoxin level< 1.000 Eu/µg
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Purity>95% by SDS-PAGE .
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FormLiquid
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Concentration information loading...
Preparation and Storage
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Stability and Storage
Shipped on Dry Ice. Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
pH: 7.5
Constituents: 0.24% Tris, 20% Glycerol, 0.02% DTT
General Info
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Alternative names
- ASF/SF2 associated protein p32
- C1q globular domain binding protein
- C1qBP
see all -
FunctionBinds to the globular "heads" of C1Q thus inhibiting C1 activation.
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Sequence similaritiesBelongs to the MAM33 family.
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Cellular localizationMitochondrion matrix. Nucleus. Might also be nuclear in some cell types.
- Information by UniProt
Datasheets and documents
References
ab172818 has not yet been referenced specifically in any publications.