Anti-NNMT Polyclonal Antibody (CABT-L2230) Knockout Validated

Rabbit Anti-Human NNMT (Met1~Arg258) Polyclonal Antibody for WB


Host Species
Antibody Isotype
Species Reactivity
Recombinant fragment corresponding to human NNMT (Met1~Arg258)


Application Notes
Recommended dilution: WB: 0.5-2 ug/ml
*Suggested working dilutions are given as a guide only. It is recommended that the user titrates the product for use in their own experiment using appropriate negative and positive controls.

Data Examples

Knockout Varification: Lane 1: Wild-type A549 cell lysate. Lane 2: NNMT knockout A549 cell lysate. Predicted MW: 30kd, Observed MW: 30kd
Figure. Western Blot. Sample. Lane1: Human Hela Cells; Lane2: Human A549 Cells; Lane3: Human U2OS Cells.
Western Blot. Sample. Human A549 cell lysate.
Western Blot. Sample. Human U2OS cell lysate.


Alternative Names
Entrez Gene ID
UniProt ID

Product Background

Biological oxidations; Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD); Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD); Defective GGT1 causes Glutathionuria (GLUTH); Defective GSS causes Glutathione synthetase deficiency (GSS deficiency); Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD); Defective OPLAH causes 5-oxoprolinase deficiency (OPLAHD); Defective SLC35D1 causes


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Katayama, K; Sasaki, T; et al. Insertional mutation in the Golgb1 gene is associated with osteochondrodysplasia and systemic edema in the OCD rat. BONE 49:1027-1036(2011).

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