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Mouse Anti-SORD Recombinant Antibody (CBXS-3686) (CBMAB-S0961-CQ)


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Summary

Host Animal
Mouse
Specificity
Human
Clone
CBXS-3686
Antibody Isotype
IgG1
Application
IHC, IHC-P, WB

Basic Information

Immunogen
Protein expressed in 293T cell transfected with human SORD expression vector
Specificity
Human
Antibody Isotype
IgG1
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS, pH 7.3, 1% BSA, 50% glycerol
Preservative
0.02% sodium azide
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
Sorbitol Dehydrogenase
Introduction
Sorbitol dehydrogenase (SORD; EC 1.1.1.14) catalyzes the interconversion of polyols and their corresponding ketoses, and together with aldose reductase (ALDR1; MIM 103880), makes up the sorbitol pathway that is believed to play an important role in the development of diabetic complications (summarized by Carr and Markham, 1995 [PubMed 8535074]). The first reaction of the pathway (also called the polyol pathway) is the reduction of glucose to sorbitol by ALDR1 with NADPH as the cofactor. SORD then oxidizes the sorbitol to fructose using NAD(+) cofactor.
Entrez Gene ID
6652
UniProt ID
Q00796
Alternative Names
Sorbitol Dehydrogenase; L-Iditol 2-Dehydrogenase; EC 1.1.1.14; Epididymis Secretory Sperm Binding Protein Li 95n; HEL-S-95n; EC 1.1.1; SORD1;
Function
Polyol dehydrogenase that catalyzes the reversible NAD+-dependent oxidation of various sugar alcohols. Is mostly active with D-sorbitol (D-glucitol), L-threitol, xylitol and ribitol as substrates, leading to the C2-oxidized products D-fructose, L-erythrulose, D-xylulose, and D-ribulose, respectively (PubMed:3365415).
Is a key enzyme in the polyol pathway that interconverts glucose and fructose via sorbitol, which constitutes an important alternate route for glucose metabolism. The polyol pathway is believed to be involved in the etiology of diabetic complications, such as diabetic neuropathy and retinopathy, induced by hyperglycemia (PubMed:12962626, PubMed:29966615, PubMed:25105142).
May play a role in sperm motility by using sorbitol as an alternative energy source for sperm motility (PubMed:16278369).
May have a more general function in the metabolism of secondary alcohols since it also catalyzes the stereospecific oxidation of (2R,3R)-2,3-butanediol. To a lesser extent, can also oxidize L-arabinitol, galactitol and D-mannitol and glycerol in vitro. Oxidizes neither ethanol nor other primary alcohols. Cannot use NADP+ as the electron acceptor (PubMed:3365415).
Biological Process
Biological Process flagellated sperm motilityISS:UniProtKB
Biological Process fructose biosynthetic processManual Assertion Based On ExperimentIDA:UniProtKB
Biological Process glucose metabolic processManual Assertion Based On ExperimentTAS:UniProtKB
Biological Process glucuronate catabolic process to xylulose 5-phosphateIEA:Ensembl
Biological Process L-xylitol catabolic processManual Assertion Based On ExperimentIDA:UniProtKB
Biological Process L-xylitol metabolic processManual Assertion Based On ExperimentIDA:UniProtKB
Biological Process response to cadmium ionIEA:Ensembl
Biological Process response to copper ionIEA:Ensembl
Biological Process response to hormoneIEA:Ensembl
Biological Process response to nutrient levelsIEA:Ensembl
Biological Process response to osmotic stressIEA:Ensembl
Biological Process response to xenobiotic stimulusIEA:Ensembl
Biological Process sorbitol catabolic processManual Assertion Based On ExperimentIDA:UniProtKB
Cellular Location
Mitochondrion membrane
Cell projection, cilium, flagellum
Associated with mitochondria of the midpiece and near the plasma membrane in the principal piece of the flagellum. Also found in the epididymosome, secreted by the epididymal epithelium and that transfers proteins from the epididymal fluid to the sperm surface.
Involvement in disease
Sorbitol dehydrogenase deficiency with peripheral neuropathy (SORDD):
An autosomal recessive disorder characterized by motor axonal neuropathy, slowly progressive distal muscle weakness mainly affecting the lower limbs, difficulty walking, and increased serum sorbitol. Additional variable features are distal sensory impairment, upper limb tremor, scoliosis, and mild hearing loss.
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For research use only. Not intended for any clinical use.

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