SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
ALG12-ZBED4-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
ALG12-ZBED4-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
Gene Symbol : ZBED4
Gene Name : Zinc finger BED-type containing 4
Chromosome : CHR 22: 498,538,48-498,900,77
Locus : 22q13.33
This gene encodes a member of the glycosyltransferase 22 family. The encoded protein catalyzes the addition of the eighth mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2)) required for protein glycosylation. Mutations in this gene have been associated with congenital disorder of glycosylation type Ig (CDG-Ig)characterized by abnormal N-glycosylation. [provided by RefSeq, Jul 2008]
Gene Symbol : ALG12
Gene Name : ALG12, alpha-1,6-mannosyltransferase
Chromosome : CHR 22: 499,184,68-498,601,62
Locus : 22q13.33
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