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  1. Alles ansehen
  2. Polyclonal

GTX106767

MMAB antibody

Eine Lieferung in diese Region ist nicht möglich.

SKU:
GTX106767
Zusätzliche Namen:
metabolism of cobalamin associated B , ATR , CFAP23 , cblB , cob
Anwendung:
WB, IHC-P
Konzentration:
0.69 mg/ml
Physischer Zustand:
Liquid
Spezies-Reaktivität:
Human
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Hersteller:
Genetex
Host:
Rabbit
Reaktivitäten:
Human
Buffer:
PBS, 1% BSA, 20% Glycerol, 0.01% Thimerosal.
Immunogen:
Recombinant protein encompassing a sequence within the center region of human MMAB. The exact sequence is proprietary.
Uniprot:
Q96EY8
Synonyme:
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
Weitere 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. [provided by RefSeq]
Versandbedingungen:
Blue Ice