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WNT7A Rabbit pAb (bs-6645R)  
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產品編號 bs-6645R
英文名稱 WNT7A Rabbit pAb
中文名稱 原癌基因wnt7a蛋白抗體
別    名 Protein Wnt-7a; wnt 7a; Protein Wnt-7a precursor; proto-oncogene wnt7a protein; wingless-type MMTV integration site family, member 7A; WNT7A; WNT7A_HUMAN.  
Specific References  (2)     |     bs-6645R has been referenced in 2 publications.
[IF=5.738] Jianglin Wang. et al. Validation and analysis of expression, prognosis and immune infiltration of WNT gene family in non-small cell lung cancer. FRONT ONCOL. 2022; 12: 911316  WB, IHC ;  Human.  
[IF=0.375] ZHANG P et al. 5-Azacytidine and trichostatin A enhance the osteogenic differentiation of bone marrow mesenchymal stem cells isolated from steroid-induced avascular necrosis of the femoral head in rabbit. J Biosci (2019) 44:87.  WB ;  Rabbit.  
研究領域 腫瘤  信號轉導  干細胞  轉錄調節因子  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 Human,Mouse,Rat
產品應用 WB=1:500-2000,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 41 kDa
檢測分子量
細胞定位 細胞外基質 分泌型蛋白 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human WNT7A: 241-349/349 
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 Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. Signaling by Wnt-7a allows sexually dimorphic development of the mullerian ducts.

Function:
Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. Signaling by Wnt-7a allows sexually dimorphic development of the mullerian ducts (By similarity).

Subunit:
Interacts with PORCN.

Subcellular Location:
Secreted, extracellular space, extracellular matrix.

Tissue Specificity:
Expression is restricted to placenta, kidney, testis, uterus, fetal lung, and fetal and adult brain.

DISEASE:
Defects in WNT7A are the cause of limb pelvis hypoplasia aplasia syndrome (LPHAS) [MIM:276820]. A syndrome of severe deficiency of the extremities due to hypo- or aplasia of one or more long bones of one or more limbs. Pelvic manifestations include hip dislocation, hypoplastic iliac bone and aplastic pubic bones. Thoracic deformity, unusual facies and genitourinary anomalies can be present.
Defects in WNT7A are a cause of Fuhrmann syndrome (FUHRS) [MIM:228930]; also known as fibular aplasia or hypoplasia femoral bowing and poly- syn- and oligodactyly. Fuhrmann syndrome is a distinct limb-malformation disorder characterized also by various degrees of limb aplasia/hypoplasia and joint dysplasia.

Similarity:
Belongs to the Wnt family.

SWISS:
O00755

Gene ID:
7476

Database links:

Entrez Gene: 7476 Human

Entrez Gene: 533782 Cow

Entrez Gene: 607180 Dog

Entrez Gene: 100055450 Horse

Entrez Gene: 22421 Mouse

Entrez Gene: 100355697 Rabbit

Entrez Gene: 114850 Rat

Omim: 601570 Human

SwissProt: O00755 Human

SwissProt: P24383 Mouse

Unigene: 72290 Human

Unigene: 56964 Mouse



產品圖片
Sample: Brain (Mouse) Lysate at 40 ug Primary: Anti-WNT7A (bs-6645R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 41 kD Observed band size: 50 kD
Sample: Lane 1: Mouse Placenta tissue lysates Lane 2: Mouse Lung tissue lysates Lane 3: Mouse Testis tissue lysates Lane 4: Mouse Kidney tissue lysates Lane 5: Rat Placenta tissue lysates Lane 6: Rat Lung tissue lysates Lane 7: Rat Testis tissue lysates Lane 8: Rat Kidney tissue lysates Lane 9: Human Hela cell lysates Lane 10: Human A431 cell lysates Lane 11: Human SH-SY5Y cell lysates Lane 12: Human HepG2 cell lysates Primary: Anti- WNT7A (bs-6645R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 41 kDa Observed band size: 41 kDa
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