LOR 抗体
(Loricrin (LOR))
This gene encodes loricrin, a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in this gene are associated with Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases. [provided by RefSeq, Jul 2008].
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37 results
LOR
适用: 人
WB, IHC
宿主: 兔
Monoclonal
Alexa Fluor 488
Recombinant Antibody
LOR
适用: 人
WB, IHC
宿主: 兔
Monoclonal
Alexa Fluor 680
Recombinant Antibody
LOR
适用: 人
WB, IHC
宿主: 兔
Monoclonal
Alexa Fluor 350
Recombinant Antibody
LOR
适用: 人
WB, IHC
宿主: 兔
Monoclonal
Alexa Fluor 405
Recombinant Antibody
LOR
适用: 人
WB, IHC
宿主: 兔
Monoclonal
Alexa Fluor 555
Recombinant Antibody
LOR
适用: 人
WB, IHC
宿主: 兔
Monoclonal
Alexa Fluor 594
Recombinant Antibody
LOR
适用: 人
WB, IHC
宿主: 兔
Monoclonal
Alexa Fluor 647
Recombinant Antibody
LOR
适用: 人
WB, IHC
宿主: 兔
Monoclonal
Alexa Fluor 750
Recombinant Antibody
Latest Publications for our LOR 抗体
: "Immunotopographical Differences of Human Skin." in: Frontiers in immunology, Vol. 9, pp. 424, (2018) (PubMed).
: "Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis." in: Human molecular genetics, (2016) (PubMed).
: "Hemolytic complement in nonhuman primates." in: Laboratory animal science, Vol. 30, Issue 6, pp. 1026-9, (1981) (PubMed).
: "Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis." in: Human molecular genetics, (2016) (PubMed).
: "Hemolytic complement in nonhuman primates." in: Laboratory animal science, Vol. 30, Issue 6, pp. 1026-9, (1981) (PubMed).
Aliases for LOR 抗体
loricrin (LOR) 抗体loricrin (Lor) 抗体
loricrin (TVAG_146950) 抗体
loricrin (TVAG_228830) 抗体
loricrin (TVAG_228920) 抗体
loricrin (TVAG_238290) 抗体
loricrin (TVAG_035050) 抗体
loricrin (TVAG_070680) 抗体
Loricrin (Bm1_52290) 抗体
loricrin (LOC100281109) 抗体
loricrin (LOC100281170) 抗体
AI036317 抗体
LOR 抗体
RGD1559993 抗体
S77319 抗体
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