SLC1A4 Antibody

說明書

中文名稱：

SLC1A4兔多克隆抗體
貨號：

CSB-PA443704
規格：

￥1100
圖片：
The image on the left is immunohistochemistry of paraffin-embedded Human ovarian cancer tissue using CSB-PA443704(SLC1A4 Antibody) at dilution 1/70, on the right is treated with synthetic peptide. (Original magnification: ×200)

The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using CSB-PA443704(SLC1A4 Antibody) at dilution 1/70, on the right is treated with synthetic peptide. (Original magnification: ×200)

Gel: 10+12%SDS-PAGE, Lysate: 30 μg, Lane: Human liver cancer tissue, Primary antibody: CSB-PA443704(SLC1A4 Antibody) at dilution 1/1250, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 20 seconds
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

Uniprot No.：

P43007
基因名：

SLC1A4
別名：

Alanine/serine/cysteine/threonine transporter 1 antibody; ASCT-1 antibody; ASCT1 antibody; AW045657 antibody; Glutamate/neutral amino acid transporter antibody; Neutral amino acid transporter A antibody; OTTHUMP00000159933 antibody; OTTHUMP00000235138 antibody; SATT antibody; SATT_HUMAN antibody; SLC1A4 antibody; Solute carrier family 1 (glutamate/neutral amino acid transporter), member 4 antibody; Solute carrier family 1 member 4 antibody
宿主：

Rabbit
反應種屬：

Human,Mouse
免疫原：

Synthetic peptide of Human SLC1A4
免疫原種屬：

Homo sapiens (Human)
標記方式：

Non-conjugated
抗體亞型：

IgG
純化方式：

Antigen affinity purification
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
產品提供形式：

Liquid
應用范圍：

ELISA,WB,IHC

推薦稀釋比：

Application	Recommended Dilution
ELISA	1:2000-1:10000
WB	1:1000-1:5000
IHC	1:100-1:300

Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
Immunohistochemistry (IHC) Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

功能：

Transporter for alanine, serine, cysteine, and threonine. Exhibits sodium dependence.
基因功能參考文獻：
1. Results suggest that ASCT1/2 may play an important role in regulating extracellular d-serine and NMDA receptor-mediated physiological effects and that ASCT1/2 inhibitors have the potential for therapeutic benefit. PMID: 28807674
2. ANKRD50 simultaneously engages multiple parts of the SNX27-retromer-WASH complex machinery in a direct and co-operative interaction network that is needed to efficiently recycle the nutrient transporters PMID: 27909246
3. SLC1A4 deficiency should not be considered a population-specific disorder, and all patients with unexplained severe neurodevelopmental delay and the features outlined should be investigated regardless of ethnicity, as there are no known metabolic markers of this potentially treatable condition. PMID: 27193218
4. SLC1A4 is the disease causing gene of a novel neurologic disorder manifesting with significant intellectual disability, severe postnatal microcephaly, spasticity and thin corpus callosum. PMID: 26138499
5. ASCT1 is essential in brain serine transport. PMID: 26041762
6. SLC1A4 disruption may impair brain development and function by decreasing the levels of L-serine in neurons. The identification of additional families with mutations in SLC1A4 would be necessary to confirm its involvement in intellectual disability. PMID: 25930971
7. Na+ interactions with the neutral amino acid transporter ASCT1. PMID: 24808181
8. ASCT1 is able to mediate a concentrative transport of alanine, which is Na+-dependent but not coupled to the Na+ gradient PMID: 11824937
9. used as receptor by HERV-W Env glycoprotein PMID: 12050356
10. results strongly suggest that combinations of amino acid sequence changes and N-linked oligosaccharides in a critical carboxyl-terminal region of extracellular loop 2 (ECL2) control retroviral utilization of both the ASCT1 and ASCT2 receptors PMID: 12584318
11. This study revealed genetic associations of SLC1A4, SQSTM1, and EIF4EBP1 with MSA. These results may lend genetic support to the hypothesis that oxidative stress is associated with the pathogenesis of MSA. PMID: 18442140
12. SLC1A4 gene is associated with schizophrenia. PMID: 18638388
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相關疾?。?/div>
Spastic tetraplegia, thin corpus callosum, and progressive microcephaly (SPATCCM)
亞細胞定位：

Membrane; Multi-pass membrane protein. Melanosome. Note=Identified by mass spectrometry in melanosome fractions from stage I to stage IV.
蛋白家族：

Dicarboxylate/amino acid:cation symporter (DAACS) (TC 2.A.23) family, SLC1A4 subfamily
組織特異性：

Expressed mostly in brain, muscle, and pancreas but detected in all tissues examined.
數據庫鏈接：

HGNC: 10942

OMIM: 600229

KEGG: hsa:6509

STRING: 9606.ENSP00000234256

UniGene: Hs.654352

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