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Alas1 (1G11) Recombinant Rabbit mAb (bsm-52012R)  
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50ul/1400.00元
100ul/2500.00元
大包裝/詢價

產品編號 bsm-52012R
英文名稱 Alas1 (1G11) Recombinant Rabbit mAb
中文名稱 5-氨基乙酰丙酸合酶1重組兔單抗
別    名 mitochondrial; nonspecific; 5 aminolevulinate synthase; 5 aminolevulinate synthase nonspecific mitochondrial; 5 aminolevulinic acid synthase; 5-aminolevulinate synthase; 5-aminolevulinic acid synthase 1; Alas 1; ALAS 3; ALAS; ALAS H; ALAS N; ALAS-H; alaS1; ALAS3; ALASH; Aminolevulinate delta synthase 1; Aminolevulinic acid synthase 1; delta ALA synthetase; delta aminolevulinate synthase; delta-ALA synthase 1; delta-aminolevulinate synthase 1; HEM1_HUMAN; MIG 4; MIG4; Migration inducing protein 4.  
研究領域 腫瘤  心血管  細胞生物  免疫學  信號轉導  
抗體來源 Rabbit
克隆類型 Recombinant
克 隆 號 1G11
交叉反應 Human (predicted: Mouse)
產品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:50-200,IF=1:50-200,Flow-Cyt=1:100-500,ICC/IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 65 kDa
檢測分子量
細胞定位 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 recombinant human Alas1 C-terminal 200aa 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 5-aminolevulinate synthase 1 (ALAS-H) and 2 (ALAS-E) are two isoforms of ALAS, an enzyme catalyzing the first step of the heme biosynthetic pathway in mammals. The erythroid-specific isoenzyme, ALAS-E, regulates the first step of hematopoietic cell differentation and iron metabolism in the liver. ALAS-H is a housekeeping protein which mediates synthesis of early heme in the mitochondria of most cells. Succinyl CoA associates with ALAS-E in protein conformation change and translocation of ALAS-E into the mitochondria and does not interact with ALAS-H. The ALAS-E 5'-flanking region contains binding sites for nuclear activators such as GATA-1, NF-E2 and EKLF. Since the ALAS gene maps to the X chromosome, mutation of the gene leads to the pyridoxine-refractory X-linked sideroblastic anemia.

Subunit:
Homodimer.

Subcellular Location:
Mitochondrion matrix

Similarity:
Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family.

SWISS:
P13196

Gene ID:
211

Database links:

Entrez Gene: 211 Human

Entrez Gene: 11655 Mouse

Entrez Gene: 65155 Rat

Omim: 125290 Human

SwissProt: P13196 Human

SwissProt: Q8VC19 Mouse

SwissProt: P13195 Rat

Unigene: 476308 Human

Unigene: 290578 Mouse

Unigene: 97126 Rat



產品圖片
Sample: Lane 1: JAR (Human) Cell Lysate at 30 ug Lane 2: Huvec (Human) Cell Lysate at 30 ug Lane 3: Hela (Human) Cell Lysate at 30 ug Lane 4: HepG2 (Human) Cell Lysate at 30 ug Lane 5: MCF-7 (Human) Cell Lysate at 30 ug Lane 6: K562 (Human) Cell Lysate at 30 ug Lane 7: Raji (Human) Cell Lysate at 30 ug Primary: Anti-Alas1 (bsm-52012R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 71/65 kD Observed band size: 65 kD
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