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MCCC2 antibody
MCCC2
Reactivity: Human, Mouse, Rat
IF
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-MCCC2 Antibody
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Target
See all MCCC2 Antibodies
MCCC2
(Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))
Reactivity
All reactivities for MCCC2 antibodies
Human, Mouse, Rat
Host
All hosts for MCCC2 antibodies
Rabbit
Clonality
All clonalities for MCCC2 antibodies
Polyclonal
Conjugate
All conjugates for MCCC2 antibodies
This MCCC2 antibody is un-conjugated
Application
All applications for MCCC2 antibodies
Immunofluorescence (IF)
Purification
Affinity purification
Immunogen
Recombinant fusion protein of human MCCC2 (NP_071415.1).
Isotype
IgG
Top Product
Discover our top product MCCC2 Primary Antibody
Alternatives
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Application Details
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Application Notes
IF 1:50-1:100
Restrictions
For Research Use only
Handling
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Concentration
1 mg/mL
Buffer
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for MCCC2
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Target
MCCC2
(Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))
Alternative Name
MCCC2 (MCCC2 Products )
Synonyms
si:dkey-57m14.1 antibody, zgc:85685 antibody, MCCB antibody, 3-METHYLCROTONYL-COA CARBOXYLASE antibody, 3-methylcrotonyl-CoA carboxylase antibody, F28A23.210 antibody, F28A23_210 antibody, 4930552N12Rik antibody, methylcrotonoyl-CoA carboxylase 2 (beta) antibody, methylcrotonoyl-CoA carboxylase 2 antibody, methylcrotonoyl-CoA carboxylase 2 S homeolog antibody, 3-methylcrotonyl-CoA carboxylase antibody, methylcrotonoyl-Coenzyme A carboxylase 2 (beta) antibody, mccc2 antibody, MCCC2 antibody, mccc2.S antibody, Mccc2 antibody, MCCB antibody
Background
MCCC2,MCCB,This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism.
Gene ID
64087
UniProt
Q9HCC0
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