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MCCC2 antibody (C-Term)
The Rabbit Polyclonal anti-MCCC2 antibody has been validated for WB. It is suitable to detect MCCC2 in samples from Human.
Catalog No. ABIN1537373
$451.00
Plus shipping costs $50.00
80 μL ABIN2850364
400 μL ABIN1537373
80 μL ABIN2850364
400 μL ABIN1537373
Delivery in 10 to 11 Business Days
Quick Overview for MCCC2 antibody (C-Term) (ABIN1537373)
Target
See all MCCC2 Antibodies
MCCC2
(Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))
Reactivity
All reactivities for MCCC2 antibodies
Human
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
Western Blotting (WB)
Clone
RB39210
Product Details anti-MCCC2 Antibody
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Binding Specificity
All epitopes for MCCC2 antibodies
AA 468-496, C-Term
Purification
This antibody is purified through a protein A column, followed by peptide affinity purification.
Immunogen
This MCCC2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 468-496 amino acids from the C-terminal region of human MCCC2.
Isotype
Ig Fraction
Alternatives
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Application Details
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Application Notes
WB: 1:1000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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
4 °C,-20 °C
Storage Comment
MCCC2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
Expiry Date
6 months
Target Details for MCCC2
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Target
MCCC2
(Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))
Alternative Name
MCCC2
Background
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.
Molecular Weight
61333
Gene ID
64087
NCBI Accession
NP_071415
UniProt
Q9HCC0
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