Skip to content

View Spec Sheet

open_in_new
  1. Shop all
  2. Polyclonal

E-AB-19194

MMAB Polyclonal Antibody

Size

£106.20

Was £118.00

SKU:
E-AB-19194
Additional Names:
ATP:cob(I)alamin adenosyltransferase ,ATP:corrinoid adenosyltransferase,ATR ,Cob,Cob(I)alamin adenosyltransferase,Cob(I)yrinic acid a,aquocob(I)alamin vitamin B12s adenosyltransferase,c-diamide adenosyltransferase,cblB,cob(I)yrinic acid a c diamide adenos
Application:
IHC, WB
Concentration:
1.14 mg/ml
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Elabscience
Host:
Rabbit
Reactivities:
Human, Mouse
Buffer:
Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Immunogen:
Fusion protein of human MMAB
Uniprot:
Q96EY8
Synonyms:
aquocob(I)alamin vitamin B12s adenosyltransferase;ATP:cob(I)alamin adenosyltransferase;ATP:corrinoid adenosyltransferase;ATR;cblB;CFAP23;cilia and flagella associated protein 23;cob;Cob(I)alamin adenosyltransferase;cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial;cob(II)alamin adenosyltransferase;cob(II)yrinic acid a,c-diamide adenosyltransferase;cobinamide/cobalamin adenosyltransferase;corrinoid adenosyltransferase;methylmalonic aciduria (cobalamin deficiency) cblB type;methylmalonic aciduria type B protein
Extra Details:
This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found.
Shipping Conditions:
Blue Ice