SLC38A5 Antibody, Biotin conjugated
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中文名稱:
SLC38A5兔多克隆抗體, Biotin偶聯
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貨號:
CSB-PA837853LD01HU
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規格:
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其他:
產品詳情
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產品名稱:
Rabbit anti-Homo sapiens (Human) SLC38A5 Polyclonal antibody
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Uniprot No.:
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基因名:
SLC38A5
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別名:
Amino acid transporter system N2 antibody; JM 24 antibody; JM24 antibody; pp7194 antibody; S38A5 antibody; S38A5_HUMAN antibody; Slc38a5 antibody; SLC8 A5 antibody; SLC8A 5 antibody; SN 2 antibody; SN2 antibody; SNAT 5 antibody; SNAT5 antibody; Sodium coupled neutral amino acid transporter 5 antibody; Sodium coupled neutral amino acid transporter5 antibody; Sodium-coupled neutral amino acid transporter 5 antibody; Solute carrier family 38 member 5 antibody; Solute carrier family 38 member5 antibody; System N transporter 2 antibody; System N transporter2 antibody
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宿主:
Rabbit
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反應種屬:
Human
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免疫原:
Recombinant Human Sodium-coupled neutral amino acid transporter 5 protein (1-48AA)
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免疫原種屬:
Homo sapiens (Human)
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標記方式:
Biotin
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克隆類型:
Polyclonal
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抗體亞型:
IgG
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純化方式:
>95%, Protein G purified
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濃度:
It differs from different batches. Please contact us to confirm it.
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保存緩沖液:
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
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產品提供形式:
Liquid
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應用范圍:
ELISA
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Protocols:
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儲存條件:
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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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.
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用途:
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
靶點詳情
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功能:
Functions as a sodium-dependent amino acid transporter which countertransport protons. Mediates the saturable, pH-sensitive, and electrogenic cotransport of several neutral amino acids including glycine, asparagine, alanine, serine, glutamine and histidine with sodium.
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基因功能參考文獻:
- Confirmed by mRNA and protein expression, the amino acid transporters SLC7A7 and SLC38A5 showed marked differences between controls and intrauterine growth restriction/pre-eclampsia and were regulated by both diseases. In contrast, ABCA1 may play an exclusive role in the development of pre-eclempsia. PMID: 29499643
- A 50kb deletion at Xp11.23 including the two genes, SLC38A5 and FTSJ1 was found in 3 brothers with moderate to severe mental retardation. PMID: 17333282
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亞細胞定位:
Cell membrane; Multi-pass membrane protein.
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蛋白家族:
Amino acid/polyamine transporter 2 family
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組織特異性:
Predominantly expressed in stomach, brain, liver, lung and intestinal tract.
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數據庫鏈接:
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