Anti-POMGNT1 Antibody (CAB9879)
- SKU:
- CAB9879
- Product type:
- Antibody
- Application:
- WB
- Application:
- IHC
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Cell Biology
Frequently bought together:
Description
抗体名: | Anti-POMGNT1 Antibody |
抗体コード: | CAB9879 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB IHC |
反応性: | Human, Mouse, Rat |
宿主種: | Rabbit |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 411-660 of human POMGNT1 (NP_060209.3). |
申し込み: | WB IHC |
推奨希釈: | WB 1:500 - 1:2000 IHC 1:50 - 1:100 |
反応性: | Human, Mouse, Rat |
ポジティブサンプル: | SH-SY5Y, Mouse kidney, Mouse heart, Mouse brain, Rat testis |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 411-660 of human POMGNT1 (NP_060209.3). |
精製方法: | Affinity purification |
ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
アイソタイプ: | IgG |
順序: | HLLE EDDS LYCI SAWN DQGY EHTA EDPA LLYR VETM PGLG WVLR RSLY KEEL EPKW PTPE KLWD WDMW MRMP EQRR GREC IIPD VSRS YHFG IVGL NMNG YFHE AYFK KHKF NTVP GVQL RNVD SLKK EAYE VEVH RLLS EAEV LDHS KNPC EDSF LPDT EGHT YVAF IRME KDDD FTTW TQLA KCLH IWDL DVRG NHRG LWRL FRKK NHFL VVGV PASP YSVK KPPS VTPI FLEP PPKE EGAP GAPE QT |
遺伝子ID: | 55624 |
Uniprot: | Q8WZA1 |
セルラーロケーション: | Golgi apparatus membrane, Single-pass type II membrane protein |
計算された分子量: | 75kDa/84kDa |
観察された分子量: | 90kDa |
同義語: | POMGNT1, GNTI.2, GnT I.2, LGMD2O, MEB, MGAT1.2, RP76, gnT-I.2, GnTI.2 |
バックグラウンド: | This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described. |
NCBI Summary: | This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014] |
UniProt Code: | Q8WZA1 |
NCBI GenInfo Identifier: | 344313163 |
NCBI Gene ID: | 55624 |
NCBI Accession: | NP_001230695 |
UniProt Related Accession: | Q8WZA1 |
Molecular Weight: | Observed: 55 kDaPredicted: 76 kDa |
NCBI Full Name: | protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 isoform 2 |
NCBI Synonym Full Names: | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) |
NCBI Official Symbol: | POMGNT1 |
NCBI Official Synonym Symbols: | MEB; RP76; GNTI.2; LGMD2O; GnT I.2; LGMDR15; MGAT1.2; gnT-I.2 |
NCBI Protein Information: | protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 |
UniProt Protein Name: | Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 |
UniProt Synonym Protein Names: | UDP-GlcNAc:alpha-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I.2; GnT I.2 |
UniProt Gene Name: | POMGNT1 |
UniProt Entry Name: | PMGT1_HUMAN |
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