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Rabbit anti-Human GCSH Monoclonal Antibody

The antibody against GCSH was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 49-173 of human GCSH (NP_004474.2) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

ADA-15700A

The antibody against GCSH was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 49-173 of human GCSH (NP_004474.2) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

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Specifications


Cat.No ADA-15700A ClonalityMonoclonal
Host SpeciesRabbitTarget NameGCSH
Target SynonymsGCE; NKH; GCSHFormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer50% Glycerol, 0.05% BSA, PBS with 0.05% proclin300, pH7.3.Purification MethodAffinity purification
Positive Samples293T, MCF7ApplicationELISA, WB, IF/ICC

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 49-173 of human GCSH (NP_004474.2)Target SpeciesHuman
Immunogen SequenceSVRKFTEKHEWVTTENGIGTVGISNFAQEALGDVVYCSLPEVGTKLNKQDEFGALESVKAASELYSPLSGEVTEINEALAENPGLVNKSCYEDGWLIKMTLSNPSELDELMSEEAYEKYIKSIEEUniprot IDP23434
Background Information
  • Uniprot Id

    P23434

  • Target Species

    Human

  • Target Name

    GCSH

  • Target Full Name

    Glycine cleavage system H protein, mitochondrial

  • Target Function

    The glycine cleavage system catalyzes the degradation of glycine. The H protein (GCSH) shuttles the methylamine group of glycine from the P protein (GLDC) to the T protein (GCST).

  • Target Involvement

    Non-ketotic hyperglycinemia (NKH)

  • Target Subcellular Location

    Mitochondrion.

  • Target Protein Families

    GcvH family

  • Target Synonyms

    GCSHGlycine cleavage system H protein; mitochondrial; Lipoic acid-containing protein

  • Target Background

    Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH). Two transcript variants, one protein-coding and the other probably not protein-coding, have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.

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