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Rabbit Anti-MNX1/HLXB9 antibody
多克隆  |   SKU:bs-11320R

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货号:bs-3351R
¥1280
订购号:bs-11320R
¥1138.00-2900.00
货期:现货
Rabbit Anti-MNX1/HLXB9 antibody
反应物种(预测)

Chicken,Dog,Pig,Cow,Rabbit

产品应用(已验证)

WB,FCM

产品应用(可尝试)

IHC,IF,ELISA

推荐稀释比例

WB=1:500-2000,Elisa=1:5000-10000,IHC-P=1:100-500,IHC-F=1:100-500,Flow Cyt=1ug/test,IF=1:100-500,

研究领域

肿瘤,细胞生物,发育生物学,神经生物学,表观遗传学,

标签

Array

  • Positive control: RSC96
    Isotype Control Antibody: Rabbit IgG ; Secondary Antibody: Goat anti-rabbit IgG-FITC, Dilution: 1:100 in 1 X PBS containing 0.5% BSA ; Primary Antibody Dilution: 6μg in 100 μL1X PBS containing 0.5% BSA.
  • Black line : Positive blank control RSC96); Negative blank control (HL60)
    Green line : Primary Antibody (Rabbit Anti- HLXB9 antibody (bs-11320R) )
    Orange line:Isotype Control Antibody (Rabbit IgG) .
    Blue line : Secondary Antibody (Goat anti-rabbit IgG-AF488)
    RSC96(Positive)and HL60(Negative control)cells (black) were fixed with 4% PFA for 10min at room temperature, permeabilized with 90% ice-cold methanol for 20 min at -20℃, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with HLXB9 Antibody(bs-11320R)at 1:50 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2% BSA in PBS, followed by secondary antibody(blue) incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).
  • Black line : Positive blank control RSC96); Negative blank control (HL60)
    Green line : Primary Antibody (Rabbit Anti- HLXB9 antibody (bs-11320R) )
    Orange line:Isotype Control Antibody (Rabbit IgG) .
    Blue line : Secondary Antibody (Goat anti-rabbit IgG-AF488)
    RSC96(Positive)and HL60(Negative control)cells (black) were fixed with 4% PFA for 10min at room temperature, permeabilized with 90% ice-cold methanol for 20 min at -20℃, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with HLXB9 Antibody(bs-11320R)at 1:50 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2% BSA in PBS, followed by secondary antibody(blue) incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).
  • Blank control: K562.
    Primary Antibody (green line): Rabbit Anti-MNX1 antibody (bs-11320R)
    Dilution: 2μg /10^6 cells;
    Isotype Control Antibody (orange line): Rabbit IgG .
    Secondary Antibody : Goat anti-rabbit IgG-FITC
    Dilution: 0.5μg /test.
    Protocol
    The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with 90% ice-cold methanol for 20 min at -20℃. The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at room temperature .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
  • Blank control: K562.
    Primary Antibody (green line): Rabbit Anti-MNX1 antibody (bs-11320R)
    Dilution: 2μg /10^6 cells;
    Isotype Control Antibody (orange line): Rabbit IgG .
    Secondary Antibody : Goat anti-rabbit IgG-FITC
    Dilution: 0.5μg /test.
    Protocol
    The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with 90% ice-cold methanol for 20 min at -20℃. The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at room temperature .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
  • Sample:
    Lane 1: Pancreas (Mouse) Lysate at 40 ug
    Lane 2: Pancreas (Rat) Lysate at 40 ug
    Primary: Anti-MNX1/HLXB9 (bs-11320R) at 1/1000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 55 kD
    Observed band size: 55 kD

产品信息

RRID:RRID
产品名称:Rabbit Anti-MNX1/HLXB9 antibody
别名: HB9/HLXB9; HB 9; HB9; HLXB 9; HLXB9; Homeo box HB9; Homeobox HB9; Homeobox protein HB9; HOXHB9; MNX1; MNX1_HUMAN; Motor neuron and pancreas homeobox protein 1; Sacral agenesis autosomal dominant (Currarino triad); SCRA 1; SCRA1; SCRA1; HOXHB9.
中文名称:运动神经元及胰腺同源蛋白1抗体
英文名称:Rabbit Anti-MNX1/HLXB9 antibody
抗体来源: Rabbit
克隆类型:多克隆
细胞定位:细胞核
性 状:Liquid
亚 型:IgG
纯化方法:affinity purified by Protein A
保存条件:Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

免疫原信息

免 疫 原:KLH conjugated synthetic peptide derived from human HLXB9
抗原表位:231-330/401
SWISS:P50219
Gene ID :3110
Human Gene ID:3110

产品介绍

The HB9 homeobox transcription factor regulates gene expression during embryonic development and also in specific adult tissues. HB9 gene mutations are implicated in Curriano syndrome, which is characterized by a triad consisting of a presacral tumor, sacral agenesis and anorectal malformation. In human bone marrow cells, HB9 expression directly correlates with CD34 expression. Furthermore, HB9 expression increases in CD34+ cells that are treated with IL-3 and granulocyte macrophage-colony-stimulating factor. Early in murine development, HB9 is expressed in pancreatic buds (dorsal and ventral) with subsequent expression in differentiating beta cells in the islets of Langerhans. The dorsal lobe of the pancreas fails to form in HB9(-) mice; the resultant pancreas has smaller islets of Langerhans and less beta cells than normal pancreas. The HB9 gene is expressed in the human adult pancreas. In the developing vertebrate embryo, the HB9 gene plays an essential role in motor neuron differentiation. The motor columns of HB9(-) mice are disorganized, lacking phrenic and abducens nerves and exhibiting intercostal nerve defects.
Function:Putative transcription factor involved in pancreas development and function.
Subcellular Location:Nucleus.
Tissue Specificity:Expressed in lymphoid and pancreatic tissues.
DISEASE:Defects in MNX1 are a cause of Currarino syndrome (CURRAS) [MIM:176450]. The triad of a presacral tumor, sacral agenesis and anorectal malformation constitutes the Currarino syndrome which is caused by dorsal-ventral patterning defects during embryonic de
Similarity:Contains 1 homeobox DNA-binding domain.
Important Note:This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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