多克隆抗体

MYO5B rabbit Polyclonal Antibody

MYO5B抗体
MYO5B抗体应用:WB 1:500-2000 ELISA 1:5000-20000myosin VB(MYO5B) Homo sapiens The protein encoded by this gene, together with other proteins, may be involved in plasma membrane recycling. Mutations in this gene are associated with microvillous inclusion disease. [provided by RefSeq, Sep 2009],

LRRDN rabbit Polyclonal Antibody

LRRDN抗体
LRRDN抗体应用:WB 1:500-2000

LRRK2 rabbit Polyclonal Antibody

LRRK2抗体
LRRK2抗体应用:IHC-p 1:50-300leucine rich repeat kinase 2(LRRK2) Homo sapiens This gene is a member of the leucine-rich repeat kinase family and encodes a protein with an ankryin repeat region, a leucine-rich repeat (LRR) domain, a kinase domain, a DFG-like motif, a RAS domain, a GTPase domain, a MLK-like domain, and a WD40 domain. The protein is present largely in the cytoplasm but also associates with the mitochondrial outer membrane. Mutations in this gene have been associated with Parkinson disease-8. [provided by RefSeq, Jul 2008],

LRRN1 rabbit Polyclonal Antibody

LRRN1抗体
LRRN1抗体应用:WB 1:500-2000 ELISA 1:5000-20000similarity:Contains 1 fibronectin type-III domain.,similarity:Contains 1 Ig-like C2-type (immunoglobulin-like) domain.,similarity:Contains 11 LRR (leucine-rich) repeats.,

LRRT1 rabbit Polyclonal Antibody

LRRT1抗体
LRRT1抗体应用:WB 1:500-2000

LRRT2 rabbit Polyclonal Antibody

LRRT2抗体
LRRT2抗体应用:WB 1:500-2000

LRSM1 rabbit Polyclonal Antibody

LRSM1抗体
LRSM1抗体应用:WB 1:500-2000 ELISA 1:5000-20000leucine rich repeat and sterile alpha motif containing 1(LRSAM1) Homo sapiens This gene encodes a ring finger protein involved in a variety of functions, including regulation of signaling pathways and cell adhesion, mediation of self-ubiquitylation, and involvement in cargo sorting during receptor endocytosis. Mutations in this gene have been associated with Charcot-Marie-Tooth disease. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jan 2012],

LS14A rabbit Polyclonal Antibody

LS14A抗体
LS14A抗体应用:WB 1:500-2000 ELISA 1:5000-20000LSM14A, mRNA processing body assembly factor(LSM14A) Homo sapiens Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Mar 2008],

LSHB rabbit Polyclonal Antibody

LSHB抗体
LSHB抗体应用:WB 1:500-2000 ELISA 1:5000-20000luteinizing hormone beta polypeptide(LHB) Homo sapiens This gene is a member of the glycoprotein hormone beta chain family and encodes the beta subunit of luteinizing hormone (LH). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biological specificity. LH is expressed in the pituitary gland and promotes spermatogenesis and ovulation by stimulating the testes and ovaries to synthesize steroids. The genes for the beta chains of chorionic gonadotropin and for luteinizing hormone are contiguous on chromosome 19q13.3. Mutations in this gene are associated with hypogonadism which is characterized by infertility and pseudohermaphroditism. [provided by RefSeq, Jul 2008],

LSM1 rabbit Polyclonal Antibody

LSM1抗体
LSM1抗体应用:WB 1:500-2000 ELISA 1:5000-20000LSM1 homolog, mRNA degradation associated(LSM1) Homo sapiens This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Increased expression of this gene may play a role in cellular transformation and the progression of several malignancies including lung cancer, mesothelioma and breast cancer. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, Nov 2011],
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