Thermo Fisher Scientific MMAA Monoclonal Antibody (OTI3G5)
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Applications
Tested Dilution
Publications
Western Blot (WB)
1:2,000
Immunohistochemistry (Paraffin) (IHC (P))
1:150
Immunocytochemistry (ICC/IF)
1:100
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG2a
Class
Monoclonal
Type
Antibody
Clone
OTI3G5
Immunogen
Full length human recombinant protein of MMAA produced in HEK293T cell if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
MMAA,
uniProtId:
Q8IVH4-1,
ncbiNodeId:
9606,
antigenRange:
1-418,
antigenLength:
418,
antigenImageFileName:
MA5-25384_MMAA_Q8IVH4-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-25384_MMAA_Q8IVH4-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Affinity Chromatography
Storage buffer
PBS, pH 7.3, with 1% BSA, 50% glycerol
Contains
0.02% sodium azide
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2723368
Target Information
The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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