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Rabbit Anti-PRPF38A/AP Conjugated antibody (bs-19403R-AP)
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說(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-19403R-AP
英文名稱 Rabbit Anti-PRPF38A/AP Conjugated antibody
中文名稱 堿性磷酸酶(AP)標(biāo)記的mRNA前體剪接因子Prp38抗體
別    名 2410002M20Rik; FLJ14936; MGC3320; OTTMUSP00000008592; PR38A_HUMAN; Pre mRNA splicing factor 38A; Pre-mRNA-splicing factor 38A; Prp38; PRP38 pre mRNA processing factor 38 (yeast) domain containing A; PRP38 pre mRNA processing factor 38 domain containing A; prpf38a; RGD1311129; RP23-406B13.4; RP5 965L7.1.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說(shuō) 明 書(shū) 100ul  
研究領(lǐng)域 細(xì)胞生物  表觀遺傳學(xué)  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Zebrafish, Sheep, Rhesus monkey, Gorilla, Orangutan, Xenopus tropicalis )
產(chǎn)品應(yīng)用 WB=1:50-200 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 37kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human PRPF38A
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:
HPRP18 is a 342 amino acid protein that localizes to nuclear speckles and plays a role in the second step of pre-mRNA splicing. A member of the PRP18 family, PRPF18 contains seven WD repeats and exists as two alternatively spliced isoforms which are encoded by a gene located on human chromosome 10p13. Chromosome 10 contains over 800 genes and 135 million nucleotides. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. Other chromosome 10 associated disorders include Cockayne syndrome, tetrahydrobiopterin deficiency and trisomy 10.

Function:
May be required for pre-mRNA splicing.

Subcellular Location:
Nucleus.

Similarity:
Belongs to the PRP38 family.

Database links:

Entrez Gene: 101091130 Cat

Entrez Gene: 456858 Chimpanzee

Entrez Gene: 507240 Cow

Entrez Gene: 475350 Dog

Entrez Gene: 101137881 Gorilla

Entrez Gene: 100050749 Horse

Entrez Gene: 84950 Human

Entrez Gene: 230596 Mouse

Entrez Gene: 100171974 Orangutan

Entrez Gene: 100520571 Pig

Entrez Gene: 100356051 Rabbit

Entrez Gene: 101115326 Sheep

Entrez Gene: 432312 Xenopus laevis

Entrez Gene: 549894 Xenopus tropicalis

SwissProt: Q0P5I6 Cow

SwissProt: Q8NAV1 Human

SwissProt: Q4FK66 Mouse

SwissProt: Q5RDD2 Orangutan

SwissProt: Q4FZQ6 Xenopus laevis

SwissProt: Q28H87 Xenopus tropicalis

Unigene: 5301 Human

Unigene: 157534 Mouse

Unigene: 413915 Mouse

Unigene: 54468 Xenopus laevis



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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