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Rabbit Anti-MFAP4/PE-Cy5.5 Conjugated antibody (bs-18824R-PE-Cy5.5)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@xucheq.com
訂購(gòu)QQ:  400-901-9800
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說(shuō) 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-18824R-PE-Cy5.5
英文名稱1 Rabbit Anti-MFAP4/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標(biāo)記的微絲相關(guān)蛋白4抗體
別    名 MFAP4; MFAP4_HUMAN; Microfibril-associated glycoprotein 4; Microfibrillar associated protein 4.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說(shuō) 明 書 100ul  
研究領(lǐng)域 細(xì)胞生物  免疫學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  細(xì)胞外基質(zhì)  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Dog, Cow, Horse, Rabbit, )
產(chǎn)品應(yīng)用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 26kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MFAP4
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產(chǎn)品介紹 background:
This gene encodes a protein with similarity to a bovine microfibril-associated protein. The protein has binding specificities for both collagen and carbohydrate. It is thought to be an extracellular matrix protein which is involved in cell adhesion or intercellular interactions. The gene is located within the Smith-Magenis syndrome region. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]

Function:
Could be involved in calcium-dependent cell adhesion or intercellular interactions.

Subcellular Location:
Secreted; extracellular space; extracellular matrix.

DISEASE:
MFAP4 is deleted in the Smith-Magenis syndrome (SMS) [MIM:182290].

Similarity:
Contains 1 fibrinogen C-terminal domain.

Database links:

Entrez Gene: 4239 Human

Entrez Gene: 286766 Cow

Entrez Gene: 489531 Dog

Entrez Gene: 76293 Mouse

Entrez Gene: 287382 Rat

Omim: 600596 Human

SwissProt: P55918 Cow

SwissProt: P55083 Human

SwissProt: Q9D1H9 Mouse

Unigene: 296049 Human

Unigene: 272278 Mouse



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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