MGAT2 antibody (AA 178-447)

Catalog No. ABIN6143811

The Rabbit Polyclonal anti-MGAT2 antibody (ABIN6143811) specifically detects MGAT2 in IHC and WB. The antibody is reactive with Human samples.

Quick Overview for MGAT2 antibody (AA 178-447) (ABIN6143811)

Target: MGAT2 (Mannosyl (Alpha-1,6-)-Glycoprotein beta-1,2-N-Acetylglucosaminyltransferase (MGAT2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MGAT2 antibody is un-conjugated

Application: Immunohistochemistry (IHC), Western Blotting (WB)

Product Details anti-MGAT2 Antibody

Binding Specificity: AA 178-447

Sequence: PFSIQLYPNE FPGSDPRDCP RDLPKNAALK LGCINAEYPD SFGHYREAKF SQTKHHWWWK LHFVWERVKI LRDYAGLILF LEEDHYLAPD FYHVFKKMWK LKQQECPECD VLSLGTYSAS RSFYGMADKV DVKTWKSTEH NMGLALTRNA YQKLIECTDT FCTYDDYNWD WTLQYLTVSC LPKFWKVLVP QIPRIFHAGD CGMHHKKTCR PSTQSAQIES LLNNNKQYMF PETLTISEKF TVVAISPPRK NGGWGDIRDH ELCKSYRRLQ

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 178-447 of human MGAT2 (NP_002399.1).

Isotype: IgG

Application Details

Application Notes: WB,1:200 - 1:2000,IHC,1:50 - 1:200

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for MGAT2

Target: MGAT2 (Mannosyl (Alpha-1,6-)-Glycoprotein beta-1,2-N-Acetylglucosaminyltransferase (MGAT2))

Alternative Name: MGAT2

Background: The product of this gene is a Golgi enzyme catalyzing an essential step in the conversion of oligomannose to complex N-glycans. The enzyme has the typical glycosyltransferase domains: a short N-terminal cytoplasmic domain, a hydrophobic non-cleavable signal-anchor domain, and a C-terminal catalytic domain. Mutations in this gene may lead to carbohydrate-deficient glycoprotein syndrome, type II. The coding region of this gene is intronless. Transcript variants with a spliced 5' UTR may exist, but their biological validity has not been determined.,MGAT2,CDG2A,CDGS2,GLCNACTII,GNT-II,GNT2,alpha-1,MGAT2

Molecular Weight: 51 kDa

Gene ID: 4247

UniProt: Q10469