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Mouse Monoclonal RBP4 antibody [4C2] (STJ98356)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, IHC, IF, FC, ELISA
Recommended dilution: WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; FC 1:200-1:400; ELISA 1:10000
Recommended protocols: check protocols
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Check alternative names for the antibodyExpand
RBP4 antibody, PRO2222 antibody,|OTTHUMP00000020114 antibody|OTTHUMP00000020115 antibody|OTTHUMP00000020116 antibody|Plasma retinol binding protein 4 antibody|Plasma retinol-binding protein antibody|Plasma retinol-binding protein(1-176) antibody|PRBP antibody|PRO2222 antibody|RBP antibody|RBP4 antibody|RDCCAS antibody|RET4_HUMAN antibody|Retinol binding protein 4 antibody|Retinol binding protein 4 interstitial antibody|Retinol binding protein 4 plasma antibody|Anti-RBP4 antibody [EP3657] (ab109193)
SCBT cat No: sc-69795|sc-27792|sc-48384|sc-46688|sc-25850|
RBP4 Monoclonal Antibody
|Catalogue No.|| |
RBP4 Monoclonal Antibody detects endogenous levels of RBP4 protein.
Purified recombinant fragment of human RBP4 expressed in E Coli
WB, IHC, IF, FC, ELISA
|Recommended dilution|| |
WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; FC 1:200-1:400; ELISA 1:10000
RBP4 Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.
RBP4 Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Retinol-binding protein 4 antibody, Plasma retinol-binding protein antibody, PRBP antibody, RBP antibody
|Protein names|| |
Retinol-binding protein 4 , Plasma retinol-binding protein , PRBP , RBP
|Protein function|| |
Delivers retinol from the liver stores to the peripheral tissues. In plasma, the RBP-retinol complex interacts with transthyretin, this prevents its loss by filtration through the kidney glomeruli.
|Involvement in disease|| |
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome (RDCCAS) [MIM:615147]: A disease characterized by retinal degeneration, ocular colobomas involving both the anterior and posterior segment, impaired night vision and loss of visual acuity. Additional characteristic features include developmental abnormalities and severe acne. . Note: The disease is caused by mutations affecting the gene represented in this entry. Loss of functional RBP4 protein results in serum retinol deficiency. Lack of normal levels of retinol impairs the visual cycle leading to night blindness at early stages; prolonged deficiency may lead to retinal degeneration. Additionally, retinol deficiency may result in dry skin, increased susceptibility to infection and acne (PubMed:23189188). .; Microphthalmia, isolated, with coloboma, 10 (MCOPCB10) [MIM:616428]: A disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues. Ocular abnormalities like opacities of the cornea and lens, scaring of the retina and choroid, and other abnormalities may also be present. Ocular colobomas are a set of malformations resulting from abnormal morphogenesis of the optic cup and stalk, and the fusion of the fetal fissure (optic fissure). . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the calycin superfamily. Lipocalin family.
|Protein cellular localization|| |
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St John’s Laboratory Ltd.
|Product type|| |
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