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Home >Products> Reagents >Other Reagents> Human CHODL Protein, His tag
Human CHODL Protein, His tag
Human CHODL Protein, His tag
Origin of place Singapore
Model S0A0155-25μg
Supplier ANT BIO PTE.LTD.
Price 235
Hits 0
Updated 8/25/2025
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Product Specification


SpeciesHuman
SynonymsChondrolectin, Transmembrane protein MT75, C21orf68, PRED12
AccessionQ9H9P2
Amino Acid Sequence

Protein sequence (Q9H9P2, Arg22-Ala211, with C-His tag) RRVVSGQKVCFADFKHPCYKMAYFHELSSRVSFQEARLACESEGGVLLSLENEAEQKLIESMLQNLTKPGTGISDGDFWIGLWRNGDGQTSGACPDLYQWSDGSNSQYRNWYTDEPSCGSEKCVVMYHQPTANPGLGGPYLYQWNDDRCNMKHNYICKYEPEINPTAPVEKPYLTNQPGDTHQNVVVTEA

Expression SystemHEK293
Molecular WeightPredicted MW: 23.2 kDa Observed MW: 34 kDa
Purity>95% by SDS-PAGE
Endotoxin<0.1EU/μg
ConjugationUnconjugated
Tagwith C-His tag
Physical AppearanceLyophilized Powder
Storage BufferLyophilized from a 0.2 μm filtered solution of 0.2M PBS, pH7.4.
ReconstitutionReconstitute 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

Chondrolectin is a type I membrane protein with a carbohydrate recognition domain characteristic of C-type lectins in its extracellular portion. This protein has been shown to localise to the perinucleus. The exact function of chondrolectin is unknown but it has been shown to be a marker of fast motor neurons in mice, and is involved in motor neuron development and growth in zebrafish (Danio rerio). Furthermore, human chondrolectin has been shown to localise to motor neurons within the spinal cord. Chondrolectin is alternatively spliced in the spinal cord of mouse models of the neuromuscular disease, spinal muscular atrophy (SMA), which predominantly affects lower motor neurons. Increased levels of chondrolectin in a zebrafish model of SMA results in significant improvements in disease-related motor neuron defects.

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