Metabolism Antibodies 1
Anti-HBS1L Antibody (CAB10037)
- SKU:
- CAB10037
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Metabolism
Description
Antibody Name: | Anti-HBS1L Antibody |
Antibody SKU: | CAB10037 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB |
Reactivity: | Human, Mouse |
Host Species: | Rabbit |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human HBS1L (NP_006611.1). |
Application: | WB |
Recommended Dilution: | WB 1:500 - 1:1000 |
Reactivity: | Human, Mouse |
Positive Samples: | NIH/3T3, Mouse pancreas |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human HBS1L (NP_006611.1). |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | MARH RNVR GYNY DEDF EDDD LYGQ SVED DYCI SPST AAQF IYSR RDKP SVEP VEEY DYED LKES SNSV SNHQ LSGF DQAR LYSC LDHM REVL GDAV PDEI LIEA VLKN KFDV QKAL SGVL EQDR VQSL KDKN EATV STGK IAKG KPVD SQTS RSES EIVP KVAK MTVS GKKQ TMGF EVPG VSSE ENGH SFHT PQKG PPIE DAIA SSDV LETA SKSA NPPH TIQA SEEQ SSTP APVK KSGK LRQQ IDVK AELE KRQG GKQL |
Gene ID: | 10767 |
Uniprot: | Q9Y450 |
Cellular Location: | |
Calculated MW: | 70kDa/75kDa |
Observed MW: | 75kDa |
Synonyms: | HBS1L, EF-1a, ERFS, HBS1, HSPC276, eRF3c |
Background: | This gene encodes a member of the GTP-binding elongation factor family. It is expressed in multiple tissues with the highest expression in heart and skeletal muscle. The intergenic region of this gene and the MYB gene has been identified to be a quantitative trait locus (QTL) controlling fetal hemoglobin level, and this region influnces erythrocyte, platelet, and monocyte counts as well as erythrocyte volume and hemoglobin content. DNA polymorphisms at this region associate with fetal hemoglobin levels and pain crises in sickle cell disease. A single nucleotide polymorphism in exon 1 of this gene is significantly associated with severity in beta-thalassemia/Hemoglobin E. Multiple alternatively spliced transcript variants encoding different protein isoforms have been found for this gene. |
UniProt Protein Function: | HBS1: a member of the GTP-binding elongation factor family. It is expressed in multiple tissues with the highest expression in heart and skeletal muscle. The intergenic region of this gene and the MYB gene has been identified to be a quantitative trait locus (QTL) controlling fetal hemoglobin level, and this region influnces erythrocyte, platelet, and monocyte counts as well as erythrocyte volume and hemoglobin content. DNA polymorphisms at this region associate with fetal hemoglobin levels and pain crises in sickle cell disease. A single nucleotide polymorphism in exon 1 of this gene is significantly associated with severity in beta-thalassemia/Hemoglobin E. Multiple alternatively spliced transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, May 2009] |
UniProt Protein Details: | Protein type:Translation; Translation elongation; RNA-binding Chromosomal Location of Human Ortholog: 6q23.3 Cellular Component: intracellular; membrane Molecular Function:GTPase activity Biological Process: ribosome disassembly; signal transduction; translation |
NCBI Summary: | This gene encodes a member of the GTP-binding elongation factor family. It is expressed in multiple tissues with the highest expression in heart and skeletal muscle. The intergenic region of this gene and the MYB gene has been identified to be a quantitative trait locus (QTL) controlling fetal hemoglobin level, and this region influnces erythrocyte, platelet, and monocyte counts as well as erythrocyte volume and hemoglobin content. DNA polymorphisms at this region associate with fetal hemoglobin levels and pain crises in sickle cell disease. A single nucleotide polymorphism in exon 1 of this gene is significantly associated with severity in beta-thalassemia/Hemoglobin E. Multiple alternatively spliced transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, May 2009] |
UniProt Code: | Q9Y450 |
NCBI GenInfo Identifier: | 68566500 |
NCBI Gene ID: | 10767 |
NCBI Accession: | Q9Y450.1 |
UniProt Secondary Accession: | Q9Y450,Q4VX89, Q4VX90, Q5T7G3, Q8NDW9, Q9UPW3, B7Z365 |
UniProt Related Accession: | Q9Y450 |
Molecular Weight: | 70,625 Da |
NCBI Full Name: | HBS1-like protein |
NCBI Synonym Full Names: | HBS1 like translational GTPase |
NCBI Official Symbol: | HBS1L |
NCBI Official Synonym Symbols: | ERFS; HBS1; EF-1a; eRF3c; HSPC276 |
NCBI Protein Information: | HBS1-like protein |
UniProt Protein Name: | HBS1-like protein |
UniProt Synonym Protein Names: | ERFS |
Protein Family: | HBS1-like protein |
UniProt Gene Name: | HBS1L |
UniProt Entry Name: | HBS1L_HUMAN |
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