Anti-GLUL Antibody (CAB5437)[KO Validated]
- SKU:
- CAB5437
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cardiovascular
Frequently bought together:
Description
抗体名: | Anti-GLUL Antibody [KO Validated] |
抗体コード: | CAB5437 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB IHC IF |
反応性: | Human, Mouse, Rat |
宿主種: | Rabbit |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-373 of human GLUL (NP_001028228.1). |
申し込み: | WB IHC IF |
推奨希釈: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200 |
反応性: | Human, Mouse, Rat |
ポジティブサンプル: | K-562, U-87MG, Mouse intestine, Mouse kidney |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-373 of human GLUL (NP_001028228.1). |
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: | MTTS ASSH LNKG IKQV YMSL PQGE KVQA MYIW IDGT GEGL RCKT RTLD SEPK CVEE LPEW NFDG SSTL QSEG SNSD MYLV PAAM FRDP FRKD PNKL VLCE VFKY NRRP AETN LRHT CKRI MDMV SNQH PWFG MEQE YTLM GTDG HPFG WPSN GFPG PQGP YYCG VGAD RAYG RDIV EAHY RACL YAGV KIAG TNAE VMPA QWEF QIGP CEGI SMGD HLWV ARFI LHRV CEDF GVIA TFDP KPIP GNWN GAGC HTNF STKA MREE NGLK YIEE AIEK LSKR HQYH IRAY DPKG GLDN ARRL TGFH ETSN INDF SAGV ANRS ASIR IPRT VGQE KKGY FEDR RPSA NCDP FSVT EALI RTCL LNET GDEP FQYK N |
遺伝子ID: | 2752 |
Uniprot: | P15104 |
セルラーロケーション: | Cytoplasm, Mitochondrion |
計算された分子量: | 42kDa |
観察された分子量: | 40kDa |
同義語: | GLNS, GS, PIG43, PIG59, GLUL |
バックグラウンド: | The protein encoded by this gene belongs to the glutamine synthetase family. It catalyzes the synthesis of glutamine from glutamate and ammonia in an ATP-dependent reaction. This protein plays a role in ammonia and glutamate detoxification, acid-base homeostasis, cell signaling, and cell proliferation. Glutamine is an abundant amino acid, and is important to the biosynthesis of several amino acids, pyrimidines, and purines. Mutations in this gene are associated with congenital glutamine deficiency, and overexpression of this gene was observed in some primary liver cancer samples. There are six pseudogenes of this gene found on chromosomes 2, 5, 9, 11, and 12. Alternative splicing results in multiple transcript variants. |
UniProt Protein Function: | GLUL: This enzyme has 2 functions: it catalyzes the production of glutamine and 4-aminobutanoate (gamma-aminobutyric acid, GABA), the latter in a pyridoxal phosphate-independent manner. Essential for proliferation of fetal skin fibroblasts. Defects in GLUL are the cause of congenital systemic glutamine deficiency (CSGD). CSGD is a rare developmental disorder with severe brain malformation resulting in multi-organ failure and neonatal death. Glutamine is largely absent from affected patients serum, urine and cerebrospinal fluid. Belongs to the glutamine synthetase family. |
UniProt Protein Details: | Protein type:Amino Acid Metabolism - alanine, aspartate and glutamate; Amino Acid Metabolism - arginine and proline; EC 6.3.1.2; Energy Metabolism - nitrogen; EC 4.1.1.15; Ligase Chromosomal Location of Human Ortholog: 1q31 Cellular Component: cytoplasm; cytosol; nucleus Molecular Function:glutamate-ammonia ligase activity; identical protein binding; protein binding Biological Process: amino acid biosynthetic process; cell proliferation; glutamate catabolic process; glutamine biosynthetic process; neurotransmitter uptake Disease: Glutamine Deficiency, Congenital |
NCBI Summary: | The protein encoded by this gene belongs to the glutamine synthetase family. It catalyzes the synthesis of glutamine from glutamate and ammonia in an ATP-dependent reaction. This protein plays a role in ammonia and glutamate detoxification, acid-base homeostasis, cell signaling, and cell proliferation. Glutamine is an abundant amino acid, and is important to the biosynthesis of several amino acids, pyrimidines, and purines. Mutations in this gene are associated with congenital glutamine deficiency, and overexpression of this gene was observed in some primary liver cancer samples. There are six pseudogenes of this gene found on chromosomes 2, 5, 9, 11, and 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014] |
UniProt Code: | P15104 |
NCBI GenInfo Identifier: | 1169929 |
NCBI Gene ID: | 2752 |
NCBI Accession: | P15104.4 |
UniProt Secondary Accession: | P15104,Q499Y9, Q5T9Z1, Q7Z3W4, Q8IZ17, |
UniProt Related Accession: | P15104 |
Molecular Weight: | 42,064 Da |
NCBI Full Name: | Glutamine synthetase |
NCBI Synonym Full Names: | glutamate-ammonia ligase |
NCBI Official Symbol: | GLUL |
NCBI Official Synonym Symbols: | GS; GLNS; PIG43; PIG59 |
NCBI Protein Information: | glutamine synthetase |
UniProt Protein Name: | Glutamine synthetase |
UniProt Synonym Protein Names: | Glutamate decarboxylase (EC:4.1.1.15); Glutamate--ammonia ligase |
UniProt Gene Name: | GLUL |
UniProt Entry Name: | GLNA_HUMAN |
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