Anti-KLF1, 2, 4抗体-抗体-抗体-生物在线
Anti-KLF1, 2, 4抗体

Anti-KLF1, 2, 4抗体

商家询价

产品名称: Anti-KLF1, 2, 4抗体

英文名称: KLF1, 2, 4

产品编号: YB--9526R

产品价格: null

产品产地: 中国/美国

品牌商标: Ybscience

更新时间: 2023-08-17T10:29:50

使用范围: 科研使用

上海钰博生物科技有限公司
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 Anti-KLF1, 2, 4抗体

产品编号 YB-9526R
英文名称 KLF1, 2, 4
中文名称 上皮锌指蛋白1, 2, 4抗体
别    名 Krueppel-like factor1, 2, 4; KLF1; KLF2; KLF4; KLF 1; KLF 2; KLF 4; KLF-1; KLF-2; KLF-4; AP2REP; EZF; IKLF; Kruppel-like factor 4 (gut); basic transcription element binding protein 2; basic transcription element binding protein BTEB2; BTE binding protein 2; BTEB2; CKLF; Colon krueppel like factor; EKLF; Epithelial zinc finger protein EZF; Erythroid krueppel like transcription factor; Erythroid transcription factor; GC box binding protein 2; Gklf; Gut-enriched krueppel like factor; Intestinal enriched krueppel like factor; Kruppel like factor 1 (erythroid); Kruppel-like factor 2 (lung); Lklf; Lung krueppel like factor; Gut-enriched krueppel-like factor.  
规格价格 100ul/1580元 购买    200ul/2480元 购买    大包装/询价
说 明 书 100ul  200ul
研究领域 心血管  细胞生物  免疫学  神经生物学  表观遗传学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Dog, Pig, Cow, 
产品应用 WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 IF=1:50-200 (石蜡切片需做抗原修复) 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 33kDa
细胞定位 细胞核 
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human KLF1, 2, 4:265-362/362 
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 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.
PubMed PubMed
产品介绍 background:
This gene encodes a hematopoietic-specific transcription factor that induces high-level expression of adult beta-globin and other erythroid genes. The zinc-finger protein binds to the DNA sequence CCACACCCT found in the beta hemoglobin promoter. Heterozygous loss-of-function mutations in this gene result in the dominant In(Lu) blood phenotype. [provided by RefSeq, Oct 2009].

Function:
Transcription regulator of erythrocyte development that probably serves as a general switch factor during erythropoiesis. Is a dual regulator of fetal-to-adult globin switching. Binds to the CACCC box in the beta-globin gene promoter and acts as a preferential activator of this gene. Furthermore, it binds to the BCL11A promoter and activates expression of BCL11A, which in turn represses the HBG1 and HBG2 genes. This dual activity ensures that, in most adults, fetal hemoglobin levels are low. Able to activate CD44 and AQP1 promoters. When sumoylated, acts as a transcriptional repressor by promoting interaction with CDH2/MI2beta and also represses megakaryocytic differentiation (By similarity).

Subunit:
Interacts with CBP and EP300; the interactions enhance the transactivation activity. Interacts with PCAF; the interaction does not acetylate EKLF and inhibits its transactivation activity (By similarity).

Subcellular Location:
Nucleus. Note=Colocalizes with SUMO1 in nuclear speckles.

Tissue Specificity:
Expression restricted to adult bone marrow and fetal liver. Not expressed in myeloid nor lymphoid cell lines.

Post-translational modifications:
Acetylated; can be acetylated on both Lys-274 and Lys-288. Acetylation on Lys-274 (by CBP) appears to be the major site affecting EKLF transactivation activity (By similarity).
Sumoylated; sumoylation, promoted by PIAS1, leads to repression of megakaryocyte differentiation. Also promotes the interaction with the CDH4 subunit of the NuRD repression complex (By similarity).
Phosphorylated primarily on serine residues in the transactivation domain. Phosphorylation on Thr-23 is critical for the transactivation activity (By similarity).

DISEASE:
Defects in KLF1 are the cause of congenital dyserythropoietic anemia type 4 (CDA4) [MIM:613673]. It is a blood disorder characterized by ineffective erythropoiesis and hemolysis resulting in anemia. Circulating erythroblasts and erythroblasts in the bone marrow show various morphologic abnormalities. Affected individuals with CDA4 also have increased levels of fetal hemoglobin.

Similarity:
Belongs to the krueppel C2H2-type zinc-finger protein family.
Contains 3 C2H2-type zinc fingers.

SWISS:
Q13351

Gene ID:
10661

Database links:

Entrez Gene: 10661 Human

Entrez Gene: 16596 Mouse

Omim: 600599 Human

SwissProt: Q13351 Human

SwissProt: P46099 Mouse

Unigene: 37860 Human

Unigene: 4847 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications