GDC-H | H protein of glycine decarboxylase complex (GDC)

325 €

AS05 074  |  Clonality: Polyclonal  |  Host: Rabbit  |   Reactivity: A. thaliana,P.hybrida cv. Mitchell, S. oleracea, T. aestivum, V. faba  |  cellular [compartment marker] of mitochondrial matrix


39 st
Item No:
AS05 074

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product information

The Glycine decarboxylase complex (GDC) is abundant in mitochondria of C3 leaves and functions in photorespiratory carbon recovery. GDC  enzyme can account for up to 50% of matrix protein, and is responsible for the most prominent metabolic activity in the mitochondria of illuminated leaves, photorespiration. GDC is a multienzyme complex composed of four component enzymes, the P-, H-, T-, and L-proteins and is responsible for the conversion of glycine produced in the peroxisome to serine in the mitochondria during photorespiratory cycle. The H-protein plays a key role as a mobile substrate that commutes between the other subunits, allowing its lipoic acid “arm” to visit the active sites of the other three components.


purified GDC-H protein from Spinacia oleracea

Host Rabbit
Clonality Polyclonal
Purity Total IgG
Format Lyophilized in PBS pH 7.4
Quantity 200 µg
Reconstitution For reconstitution add 200 µl of sterile water.
Storage Store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from lyophilized material adhering to the cap or sides of the tubes.
Tested applications Western blot (WB)
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Plant protein extraction buffer

Secondary antibodies

Additional information Cellular [compartment marker] of mitochondrial matrix
application information
Recommended dilution 1 : 5 000 (WB)
Expected | apparent MW

16 kDa

Confirmed reactivity Arabidopsis thaliana, Petunia hybrida cv. Mitchell, Spinacia oleracea, Triticum aestivum, Vicia faba
Predicted reactivity
Not reactive in No confirmed exceptions from predicted reactivity are currently known.
Additional information This antibody can be used on total cell extract of Arabidopsis thaliana.
Selected references Lynch et al. (2017). Multifaceted plant responses to circumvent Phe hyperaccumulation by downregulation of flux through the shikimate pathway and by vacuolar Phe sequestration. Plant J. 2017 Dec;92(5):939-950. doi: 10.1111/tpj.13730. (Petunia hybrida cv. Mitchell)
Bancel et al. (2015). Proteomic Approach to Identify Nuclear Proteins in Wheat Grain. J Proteome Res. 2015 Sep 8.
Long et al. (2015). Contributions of photosynthetic and non-photosynthetic cell types to leaf respiration in Vicia faba L. and their responses to growth temperature. Plant Cell Environ. 2015 Apr 1. doi: 10.1111/pce.12544.
Córdoba-Cañero et al. (2011). Arabidopsis ARP endonuclease functions in a branched base excision DNA repair pathway completed by LIG1. The Plant J in print

application example


15 µg of total protein from  Arabidopsis thaliana leaf extract has been loaded per lane. Primary antibody has been used in 1: 5000 dilution using standard ECL.


western blot detection using anti-GDC-H antibody

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