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Rabbit Anti-PRDM16  antibody (bs-19986R)  
~~~促銷代碼KT202411~~~
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產品編號 bs-19986R
英文名稱 Rabbit Anti-PRDM16  antibody
中文名稱 PRDM鋅指轉錄因子PRDM16抗體
別    名 CMD1LL; KIAA1675; LVNC8; MDS1/EVI1 like gene 1; MDS1/EVI1-like gene 1; MEL1; PFM 13; PFM13; PR domain containing 16; PR domain containing protein 16; PR domain zinc finger protein 16; PR domain-containing protein 16; PRD16_HUMAN; Transcription factor MEL 1; Transcription factor MEL1.  
Specific References  (2)     |     bs-19986R has been referenced in 2 publications.
[IF=6.706] Yu Wang. et al. Seabuckthorn Reverses High-Fat-Diet-Induced Obesity and Enhances Fat Browning via Activation of AMPK/SIRT1 Pathway. NUTRIENTS. 2022 Jan;14(14):2903  WB ;  Mouse.  
[IF=3.189] Tingting Li. et al. Cold exposure induces browning of bovine subcutaneous white fat in vivo and in vitro. J THERM BIOL. 2023 Feb;112:103446  WB ;  Bovine.  
研究領域 腫瘤  細胞生物  轉錄調節因子  t-淋巴細胞  鋅指蛋白  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat,Sheep,Cow,Horse)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500,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 140kDa
細胞定位 細胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human PRDM16: 701-800/1276 
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 The reciprocal translocation t(1;3)(p36;q21) occurs in a subset of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). This gene is located near the 1p36.3 breakpoint and has been shown to be specifically expressed in the t(1:3)(p36,q21)-positive MDS/AML. The protein encoded by this gene is a zinc finger transcription factor and contains an N-terminal PR domain. The translocation results in the overexpression of a truncated version of this protein that lacks the PR domain, which may play an important role in the pathogenesis of MDS and AML. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]

Function:
Binds DNA and functions as a transcriptional regulator. Functions in the differentiation of brown adipose tissue (BAT) which is specialized in dissipating chemical energy in the form of heat in response to cold or excess feeding while white adipose tissue (WAT) is specialized in the storage of excess energy and the control of systemic metabolism. Together with CEBPB, regulates the differentiation of myoblastic precursors into brown adipose cells. Functions also as a repressor of TGF-beta signaling. Isoform 4 may regulate granulocytes differentiation.

Subcellular Location:
Nucleus.

Tissue Specificity:
Expressed in uterus and kidney.

DISEASE:
Note=A chromosomal aberration involving PRDM16 is found in myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). Reciprocal translocation t(1;3)(p36;q21). Isoform 4 is specifically expressed in adult T-cell leukemia.

Similarity:
Contains 10 C2H2-type zinc fingers.
Contains 1 SET domain.

SWISS:
Q9HAZ2

Gene ID:
63976

Database links:

Entrez Gene: 63976 Human

Entrez Gene: 70673 Mouse

Entrez Gene: 100366024 Rat

Omim: 605557 Human

SwissProt: Q9HAZ2 Human

SwissProt: A2A935 Mouse

Unigene: 99500 Human

Unigene: 257785 Mouse



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