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          • Primary Antibodies ›
          • MCCC2 Antibodies

          Bioss

          MCCC2 Polyclonal Antibody

          View all (10) MCCC2 antibodies

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          Cite MCCC2 Polyclonal Antibody

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

          FIGURE: 1 / 1

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          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. {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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          MCCC2 Antibody in Western Blot (WB)
          MCCC2 Polyclonal Antibody

          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 Unconjugated 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.

          References (0)

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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

          View more View less

          Gene Aliases: 4930552N12Rik; MCCB; MCCC2

          View more View less

          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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          If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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