Anti-SLC37A4 Antibody (CAB14564)
- SKU:
- CAB14564
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Signal Transduction
Frequently bought together:
Description
抗体名: | Anti-SLC37A4 Antibody |
抗体コード: | CAB14564 |
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: | A synthetic peptide corresponding to a sequence within amino acids 300 to the C-terminus of human SLC37A4 (NP_001157752.1). |
申し込み: | WB IHC |
推奨希釈: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 |
反応性: | Human, Mouse, Rat |
ポジティブサンプル: | Mouse kidney, Rat liver |
免疫原: | A synthetic peptide corresponding to a sequence within amino acids 300 to the C-terminus of human SLC37A4 (NP_001157752.1). |
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: | RHGL LLFM MAGM TVSM YLFR VTVT SDSP KLWI LVLG AVFG FSSY GPIA LFGV IANE SAPP NLCG TSHA IVGL MANV GGFL AGLP FSTI AKHY SWST AFWV AEVI CAAS TAAF FLLR NIRT KMGR VSKK AE |
遺伝子ID: | 2542 |
Uniprot: | O43826 |
セルラーロケーション: | Endoplasmic reticulum membrane, Multi-pass membrane protein |
計算された分子量: | 46kDa/48kDa |
観察された分子量: | 46kDa |
同義語: | SLC37A4, G6PT1, G6PT2, G6PT3, GSD1b, GSD1c, GSD1d, PRO0685, TRG-19, TRG19 |
バックグラウンド: | This gene regulates glucose-6-phosphate transport from the cytoplasm to the lumen of the endoplasmic reticulum, in order to maintain glucose homeostasis. It also plays a role in ATP-mediated calcium sequestration in the lumen of the endoplasmic reticulum. Mutations in this gene have been associated with various forms of glycogen storage disease. Alternative splicing in this gene results in multiple transcript variants. |
UniProt Protein Function: | SLC37A4: Transports glucose-6-phosphate from the cytoplasm to the lumen of the endoplasmic reticulum. Forms with glucose-6- phosphatase the complex responsible for glucose production through glycogenolysis and gluconeogenesis. Hence, it plays a central role in homeostatic regulation of blood glucose levels. Defects in SLC37A4 are the cause of glycogen storage disease type 1B (GSD1B). GSD1B is a metabolic disorder characterized by impairment of terminal steps of glycogenolysis and gluconeogenesis. GSD1 patients manifest a wide range of clinical symptoms and biochemical abnormalities, including hypoglycemia, severe hepatomegaly due to excessive accumulation of glycogen, kidney enlargement, growth retardation, lactic acidemia, hyperlipidemia, and hyperuricemia. GSD1B patients also present a tendency towards infections associated with neutropenia, relapsing aphthous gingivostomatitis, and inflammatory bowel disease. Defects in SLC37A4 are the cause of glycogen storage disease type 1C (GSD1C). Defects in SLC37A4 are the cause of glycogen storage disease type 1D (GSD1D). Belongs to the major facilitator superfamily. Organophosphate:Pi antiporter (OPA) (TC 2.A.1.4) family. 2 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:Transporter; Membrane protein, integral; Membrane protein, multi-pass; Transporter, SLC family Chromosomal Location of Human Ortholog: 11q23.3 Cellular Component: endoplasmic reticulum membrane; membrane; endoplasmic reticulum; integral to membrane; integral to endoplasmic reticulum membrane Molecular Function:transporter activity; glucose-6-phosphate transmembrane transporter activity Biological Process: glucose-6-phosphate transport; transport; hexose transport; carbohydrate metabolic process; glucose metabolic process; pathogenesis; glucose transport; glucose homeostasis; transmembrane transport Disease: Glycogen Storage Disease Ic; Glycogen Storage Disease Ib |
NCBI Summary: | This gene regulates glucose-6-phosphate transport from the cytoplasm to the lumen of the endoplasmic reticulum, in order to maintain glucose homeostasis. It also plays a role in ATP-mediated calcium sequestration in the lumen of the endoplasmic reticulum. Mutations in this gene have been associated with various forms of glycogen storage disease. Alternative splicing in this gene results in multiple transcript variants.[provided by RefSeq, Aug 2009] |
UniProt Code: | O43826 |
NCBI GenInfo Identifier: | 40352813 |
NCBI Gene ID: | 2542 |
NCBI Accession: | AAH64563.1 |
UniProt Secondary Accession: | O43826,O96016, Q5J7V4, Q9UI19, Q9UNS4, |
UniProt Related Accession: | O43826 |
Molecular Weight: | 48,840 Da |
NCBI Full Name: | Solute carrier family 37 (glucose-6-phosphate transporter), member 4 |
NCBI Synonym Full Names: | solute carrier family 37 (glucose-6-phosphate transporter), member 4 |
NCBI Official Symbol: | SLC37A4 |
NCBI Official Synonym Symbols: | G6PT1; G6PT2; G6PT3; GSD1b; GSD1c; GSD1d; TRG19; TRG-19; PRO0685 |
NCBI Protein Information: | glucose-6-phosphate translocase; glucose-5-phosphate transporter; transformation-related gene 19 protein; microsomal glucose-6-phosphate transporter; glucose-6-phosphatase, transport (glucose) protein 3; glucose-6-phosphatase, transport (glucose-6-phosphate) protein 1; glucose-6-phosphatase, transport (phosphate/pyrophosphate) protein 2 |
UniProt Protein Name: | Glucose-6-phosphate translocase |
UniProt Synonym Protein Names: | Glucose-5-phosphate transporter; Solute carrier family 37 member 4; Transformation-related gene 19 protein; TRG-19 |
Protein Family: | Glucose-6-phosphate exchanger |
UniProt Gene Name: | SLC37A4 |
UniProt Entry Name: | G6PT1_HUMAN |
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