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            • Primary Antibodies ›
            • MCCC2 Antibodies

            Bioss

            MCCC2 Polyclonal Antibody

            View all (12) MCCC2 antibodies
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            Cite MCCC2 Polyclonal Antibody

            • Antibody Testing Data (1)
            Application
            MCCC2 Antibody in Western Blot (WB)
            Group 53 Created with Sketch.

            FIGURE: 1 / 1

            MCCC2 Antibody (BS-18719R) in WB

            Lane 1: Mouse kidney lysates; Lane 2: DU145 cell lysates probed with MCCC2 Polyclonal Antibody, Unconjugated (bs-18719R) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37°C.
            View Product

            MCCC2 Antibody in Western Blot (WB)

            Product Details

            BS-18719R

            Applications
            Tested Dilution
            Publications

            Western Blot (WB)

            1:1,000
            -
            Product Specifications

            Species Reactivity

            Amphibian, Human, Mouse, Rat

            Host/Isotype

            Rabbit / IgG

            Class

            Polyclonal

            Type

            Antibody

            Immunogen

            KLH conjugated synthetic peptide derived from human MCCC2, amino acids 351-450.
            View immunogen

            Conjugate

            Unconjugated

            Form

            Liquid

            Concentration

            1 mg/mL

            Purification

            Protein A

            Storage buffer

            0.01M TBS, pH 7.4, with 1% BSA, 50% glycerol

            Contains

            0.02% ProClin 300

            Storage conditions

            -20°C

            Shipping conditions

            Ambient (domestic); Wet ice (international)

            Target Information

            COX3 is a multi-pass membrane protein. It belongs to the cytochrome c oxidase subunit 3 family. Defects in COX3 are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in MT-CO3 are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.

            For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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            Cite this product

            Bioinformatics

            Protein Aliases: 3-methylcrotonyl-CoA carboxylase 2; 3-methylcrotonyl-CoA carboxylase non-biotin-containing subunit; 3-methylcrotonyl-CoA:carbon dioxide ligase subunit beta; biotin carboxylase; MCCase subunit beta; meth; methylcrotonoyl-CoA carboxylase 2 (beta); Methylcrotonoyl-CoA carboxylase beta chain, mitochondrial; methylcrotonoyl-Coenzyme A carboxylase 2 (beta); non-biotin containing subunit of 3-methylcrotonyl-CoA carboxylase; testicular secretory protein Li 29

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            Gene Aliases: 4930552N12Rik; MCCB; MCCC2

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            UniProt ID: (Human) Q9HCC0, (Rat) Q5XIT9, (Mouse) Q3ULD5

            View more View less

            Entrez Gene ID: (Human) 64087, (Rat) 361884, (Mouse) 78038

            View more View less

            Function(s)

            methylcrotonoyl-CoA carboxylase activity protein binding ATP binding nucleotide binding ligase activity ligase metabolite interconversion enzyme

            Process(es)

            leucine catabolic process biotin metabolic process branched-chain amino acid catabolic process coenzyme A metabolic process protein heterooligomerization
            It has to be done as per old AB suggested Products section.
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