Anti-p57/CDKN1C Antibody |产品详情|进口橙子视频旧款采购网

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Anti-p57/CDKN1C Antibody

品牌：Antibodies

货号：

规格：50µl

货期：

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Anti-p57/CDKN1C Antibody

商品详情参考文献相关资料

Name:	Anti-p57/CDKN1C Antibody See all p57 primary antibodies
Description:	Rabbit polyclonal antibody to p57/CDKN1C
Specificity:	CDKN1C pAb detects endogenous levels of CDKN1C protein.
Applications:	WB, IHC
Reactivity:	Human
Immunogen:	Recombinant full length Human CDKN1C.
Host:	Rabbit
Clonality:	Polyclonal
Conjugate:	Unconjugated
Molecular Weight:	~ 57 kDa
Purity:	The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Product Form:	1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.

Function:	Potent tight-binding inhibitor of several G1 cyclin/CDK complexes (cyclin E-CDK2, cyclin D2-CDK4, and cyclin A-CDK2) and, to lesser extent, of the mitotic cyclin B-CDC2. Negative regulator of cell proliferation. May play a role in maintenance of the non-proliferative state throughout life.
Tissue Specificity:	Expressed in the heart, brain, lung, skeletal muscle, kidney, pancreas and testis. Expressed in the eye. High levels are seen in the placenta while low levels are seen in the liver.
Involvement in Disease:	Beckwith-Wiedemann syndrome: A disorder characterized by anterior abdominal wall defects including exomphalos (omphalocele), pre- and postnatal overgrowth, and macroglossia. Additional less frequent complications include specific developmental defects and a predisposition to embryonal tumors. Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies: A rare condition characterized by intrauterine growth restriction, metaphyseal dysplasia, congenital adrenal hypoplasia, and genital anomalies. Patients with this condition may present shortly after birth with severe adrenal insufficiency, which can be life-threatening if not recognized early and commenced on steroid replacement therapy. Other reported features in this condition include, hypercalciuria and/or hypercalcemia, craniosesynostosis, cleft palate, and scoliosesis.
Sequence Similarities:	Belongs to the CDI family.
Cellular locations:	Nucleus.