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Recombinant Human C1qTNF5/CTRP5 His Protein

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SDS-Page: Recombinant Human C1qTNF5/CTRP5 His Protein [NBP2-77501] - 3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain.
SDS-Page: Recombinant Human C1qTNF5/CTRP5 His Protein [NBP2-77501] - 3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain.

Product Details

Summary
Reactivity HuSpecies Glossary
Applications PAGE
Concentration
0.25 mg/ml

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Recombinant Human C1qTNF5/CTRP5 His Protein Summary

Description
A recombinant protein with a N terminal His-tag and corresponding to the amino acids 16-243 of Human CTRP5/C1qTNF5.

Source: E.coli

Amino Acid Sequence: MGSSHHHHHH SSGLVPRGSH MGSHMSPPLD DNKIPSLCPG HPGLPGTPGH HGSQGLPGRD GRDGRDGAPG APGEKGEGGR PGLPGPRGDP GPRGEAGPAG PTGPAGECSV PPRSAFSAKR SESRVPPPSD APLPFDRVLV NEQGHYDAVT GKFTCQVPGV YYFAVHATVY RASLQFDLVK NGESIASFFQ FFGGWPKPAS LSGGAMVRLE PEDQVWVQVG VGDYIGIYAS IKTDSTFSGF LVYSDWHSSP VFA
Source
E. coli
Protein/Peptide Type
Recombinant Protein
Gene
C1QTNF5
Purity
>85%, by SDS-PAGE
Endotoxin Note
< 1.0 EU per 1ug of protein (determined by LAL method)

Applications/Dilutions

Dilutions
  • SDS-Page
Theoretical MW
26.4 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
20mM Tris-HCl buffer (pH8.5), 30% glycerol, 0.2M NaCl
Preservative
No Preservative
Concentration
0.25 mg/ml
Purity
>85%, by SDS-PAGE

Alternate Names for Recombinant Human C1qTNF5/CTRP5 His Protein

  • C1q and tumor necrosis factor related protein 5
  • C1qTNF5
  • Complement C1q Tumor Necrosis Factor-Related Protein 5 Precursor Variant 3
  • CTRP5
  • CTRP5LORDDKFZp586B0621
  • LORD 6
  • Myonectin 3

Background

Defects in C1QTNF5 are a cause of late-onset retinal degeneration (LORD). LORD is an autosomal dominant disorder characterized by onset in the fifth to sixth decade with night blindness and punctate yellow-white deposits in the retinal fundus, progressing to severe central and peripheral degeneration, with choroidal neovascularization and chorioretinal atrophy.; Subcellular location: Secreted

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Peptides and proteins are guaranteed for 3 months from date of receipt.

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Bioinformatics

Gene Symbol C1QTNF5