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視神經視網膜相關蛋白VAX1抗體

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中文名稱 視神經視網膜相關蛋白VAX1抗體
別    名 VAX1; VAX1_HUMAN; ventral anterior homeobox 1.  
研究領域 細胞生物  神經生物學  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, Mouse, Rat,  (predicted: Chicken, Dog, Pig, Cow, )
產品應用 WB=1:500-2000 ELISA=1:500-1000 Flow-Cyt=0.2μg/Test 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 35kDa
細胞定位 細胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human VAX1:133-200/334 
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMed PubMed
產品介紹 The homeobox DNA-binding domain is a 60 amino acid motif that is conserved among many species and functions to bind DNA via a helix-turn-helix structure, thereby playing a role in transcriptional regulation and the control of gene expression. VAX1 (ventral anterior homeobox 1) is a 334 amino acid protein that localizes to the nucleus and contains one homeobox DNA-binding domain. Expressed as multiple alternatively spliced isoforms, VAX1 is required for major tract formation and axon guidance in the developing brain and may play a role in the differentiation of various structures, including the optic stalk, the neuroretina and the pigmented epithelium. The gene encoding VAX1 maps to human chromosome 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome.

Function:
Required for axon guidance and major tract formation in the developing forebrain. May contribute to the differentiation of the neuroretina, pigmented epithelium and optic stalk.

Subcellular Location:
Nucleus.

DISEASE:
Defects in VAX1 are the cause of microphthalmia, syndromic, type 11 (MCOPS11) [MIM:614402]. A rare clinical entity including as main characteristics microphthalmia and small optic nerves, cleft lip and palate, absence of corpus callosum, hippocampal malformations, and absence of the pineal gland. Microphthalmia is a disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities.

Similarity:
Belongs to the EMX homeobox family.
Contains 1 homeobox DNA-binding domain.

SWISS:
Q5SQQ9

Gene ID:
11023

Database links:

Entrez Gene: 11023 Human

Entrez Gene: 22326 Mouse

Entrez Gene: 64571 Rat

Omim: 604294 Human

SwissProt: Q5SQQ9 Human

SwissProt: Q2NKI2 Mouse

SwissProt: Q9JM00 Rat

Unigene: 441536 Human

Unigene: 23801 Mouse

Unigene: 48764 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
 
產品圖片 Sample:
MCF-7 Cell (Human) Lysate at 40 ug
U937 Cell (Human) Lysate at 40 ug
Primary: Anti-VAX1 (bs-11496R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 35 kD
Observed band size: 36 kD
Sample: BRL-3A Cell (Rat) Lysate at 40 ug
Primary: Anti- VAX1 (bs-11496R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 35 kD
Observed band size: 37 kD
Sample: RAW264.7 Cell (Mouse) Lysate at 40 ug
Primary: Anti- VAX1 (bs-11496R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 35 kD
Observed band size: 37 kD
Sample: NIH/3T3 Cell (Mouse) Lysate at 40 ug
Primary: Anti- VAX1 (bs-11496R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 35 kD
Observed band size: 37 kD
Blank control (blue line): Hep G2 (fixed with 70% ethanol (Overnight at 4℃) and then permeabilized with 90% methanol for 20 min at -20℃).
Primary Antibody (green line): Rabbit Anti-VAX1 antibody (bs-11496R),Dilution: 0.2μg /10^6 cells;
Isotype Control Antibody (orange line): Rabbit IgG .
Secondary Antibody (white blue line): Goat anti-rabbit IgG-PE,Dilution: 1μg /test.

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