SMCR7L Gene
protein-coding GIFtS: 47
GCID: GC22P039895
|
|
Smith-Magenis syndrome chromosome region, candidate 7-like
| |
Aliases for SMCR7L gene
(According to
1HGNC,
2Entrez Gene,
3UniProtKB/Swiss-Prot,
4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc,
7Ensembl,
8DME,
9miRBase,
and/or 10fRNAdb) About This Section
|
| Aliases |
|---|
| Smith-Magenis Syndrome Chromosome Region, Candidate 7-Like1 2 | | FLJ202321 | | Mitochondrial Dynamic Protein Of 51 KDa2 3 | | MiD511 | | Mitochondrial Elongation Factor 12 3 | | HSU792522 | | Smith-Magenis Syndrome Chromosomal Region Candidate Gene 7 Protein-Like2 3 | | DJ1104E15.31 | | MID512 3 | | Mitochondrial Dynamic Protein MID512 | | MIEF12 3 | | |
Export aliases for SMCR7L gene to outside databasesPrevious GC identifers: GC22P038228 GC22P022862 |
Summaries for SMCR7L gene(According to Entrez Gene,
Tocris Bioscience,
Wikipedia's
Gene Wiki,
PharmGKB,
UniProtKB/Swiss-Prot,
and/or
UniProtKB/TrEMBL)
About This Section
| UniProtKB/Swiss-Prot: MID51_HUMAN, Q9NQG6Function: Mitochondrial outer membrane protein which regulates mitochondrial morphology. Mitochondrial morphology iscontrolled by two opposites processes: fusion and fission. Seems to have a key role in inhibiting DNM1L-inducedmitochondrial fission Gene Wiki entry for SMCR7L
|
Genomic Views for SMCR7L gene
(According to
GeneLoc and/or
HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to
UCSC (hg19) and
Ensembl (release 69),
Regulatory elements and Epigenetics data according to
QIAGEN,
SABiosciences, and/or
SwitchGear Genomics) About This Section
| RefSeq DNA sequence:- NC_000022.10 NC_018933.1 NT_011520.12
Regulatory elements: SABiosciences Regulatory transcription factor binding sites in the SMCR7L gene promoter: CREB C/EBPbeta AP-1 deltaCREB ATF6 Other transcription factors
Search SABiosciences Chromatin IP Primers for SMCR7L
Epigenetics:
|  | QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SMCR7L |
Genomic Location: Genomic View: UCSC Golden Path with GeneCards custom track
Entrez Gene cytogenetic band: 22q13 Ensembl cytogenetic band: 22q13.1 HGNC cytogenetic band: 22q13.1SMCR7L Gene in genomic location: bands according to Ensembl, locations according to
(and/or Entrez Gene and/or Ensembl if different)

GeneLoc information about chromosome 22 GeneLoc Exon Structure GeneLoc location for GC22P039895: view genomic region
(about GC identifiers)
Start:
|
39,895,437 bp from pter |
End:
|
39,914,137 bp from pter |
Size:
|
18,701 bases |
Orientation:
|
plus strand |
|
Proteins for SMCR7L gene
(According to
1UniProtKB,
HORDE,
neXtProt,
Ensembl,
and/or Reactome,
Modification sites according to 2PhosphoSitePlus,
Specific Peptides from DME,
Protein expression images according to data from SPIRE MOPED and PaxDb,
RefSeq according to NCBI,
PDB rendering according to OCA and/or Proteopedia,
Recombinant Proteins
from
EMD Millipore,
R&D Systems,
GenScript,
Enzo Life Sciences,
OriGene,
Novus Biologicals,
Sino Biological,
ProSpec, and/or
Uscn,
Biochemical Assays by
EMD Millipore,
R&D Systems,
OriGene,
GenScript,
Cell Signaling Technology,
Enzo Life Sciences, and/or
Uscn,
Ontologies according to Gene
Ontology Consortium 01 Mar 2013 and
Entrez Gene,
Antibodies by
EMD Millipore,
R&D Systems,
GenScript,
Cell Signaling Technology,
OriGene,
Novus Biologicals,
Thermo Fisher Scientific,
Abcam, and/or
Uscn)
About This Section
| UniProtKB/Swiss-Prot: MID51_HUMAN, Q9NQG6 (See
protein sequence)Recommended Name: Mitochondrial dynamic protein MID51 Size: 463 amino acids; 51293 Da
Subunit: Homodimer
Subcellular location: Mitochondrion outer membrane; Single-pass membrane protein
Secondary accessions: Q9BUI3Explore the universe of human proteins at neXtProt for SMCR7L: NX_Q9NQG6
Post-translational modifications:
View modification sites using PhosphoSitePlus2View neXtProt modification sites for NX_Q9NQG6 SMCR7L Protein expression data from MOPED and PaxDb: About this image 
 REFSEQ proteins: NP_061881.2 ENSEMBL proteins: ENSP00000385110 ENSP00000404096 ENSP00000327124 ENSP00000385191 ENSP00000390029 ENSP00000413730 Human Recombinant Protein Products for SMCR7L:
Gene Ontology (GO): 3 cellular component terms (GO ID links to tree view): About this table
SMCR7L for ontologies About GeneDecksing
SMCR7L Antibody Products: Assay Products for SMCR7L: |
Protein
Domains / Families for SMCR7L gene(According to InterPro, ProtoNet,
UniProtKB, and/or BLOCKS,
Sets of similar genes according to GeneDecks)
About This Section
|
SMCR7L for domains About GeneDecksing
1 InterPro domain/family:Graphical View of Domain Structure for InterPro Entry Q9NQG6ProtoNet protein and cluster: Q9NQG6 UniProtKB/Swiss-Prot: MID51_HUMAN, Q9NQG6Similarity: Belongs to the SMCR7 family |
Function for SMCR7L gene
(According to 1UniProtKB,
Genatlas,
LifeMap Discovery™,
IUBMB, and/or
2DME,
Human phenotypes from GenomeRNAi,
Animal models from MGI Mar 06 2013,
inGenious Targeting Laboratory,
bound targets from SABiosciences,
miRNA Gene Targets from miRTarBase,
shRNA from
OriGene,
Sirion Biotech,
RNAi from
EMD Millipore,
siRNAs from
OriGene,
QIAGEN,
microRNA from QIAGEN,
Gene Editing from DNA2.0,
Sirion Biotech,
Clones from EMD Millipore,
OriGene,
SwitchGear Genomics,
GenScript,
Sino Biological,
DNA2.0,
and Vector BioLabs,
Cell Lines from GenScript,
LifeMap BioReagents,
Sirion Biotech,
In Situ Hybridization Assays from Advanced Cell Diagnostics,
Ontologies according to Gene Ontology Consortium 01 Mar 2013 via
Entrez Gene.)
About This Section
| Molecular Function: UniProtKB/Swiss-Prot Summary: MID51_HUMAN, Q9NQG6Function: Mitochondrial outer membrane protein which regulates mitochondrial morphology. Mitochondrial morphology iscontrolled by two opposites processes: fusion and fission. Seems to have a key role in inhibiting DNM1L-inducedmitochondrial fission Gene Ontology (GO): 1 molecular function term (GO ID links to tree view): About this table | GO ID | Qualified GO term | Evidence | PubMed IDs |
|---|
| GO:0005515 | protein binding |
IPI | -- |
SMCR7L for ontologies About GeneDecksing
Animal Models:
Clone Products: |  | Browse Clones for the Expression of Recombinant Proteins Available from EMD Millipore | |  | OriGene Myc/DDK tagged cDNA clones in CMV expression vector in human, mouse, rat for SMCR7L (see all 3) OriGene untagged cDNA clones in CMV expression vector in human, mouse, rat for SMCR7L OriGene custom cloning services - gene synthesis, subcloning, mutagenesis,
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In Situ Assay Products: |
| Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SMCR7L |
|
Pathways & Interactions for SMCR7L gene
(Pathways according to
EMD Millipore,
R&D Systems,
Cell Signaling Technology,
KEGG,
PharmGKB,
BioSystems,
Reactome,
Tocris Bioscience,
GeneGo (Thomson Reuters),
QIAGEN,
and/or UniProtKB,
Sets of similar genes according to GeneDecks,
Interaction Networks according to
SABiosciences,
and/or STRING,
Interactions according to 1UniProtKB,
2MINT,
3I2D, and/or
4STRING,
with links to IntAct and
Ensembl,
Ontologies according to Gene Ontology Consortium 01 Mar 2013 via
Entrez Gene).
About This Section
|
Interactions:
Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for SMCR7L
STRING Interaction
Network Preview (showing 5 interactants - click image to see 6)
 5/8 Interacting proteins for SMCR7L (Q9NQG62, 3 ENSP000003271244) via UniProtKB, MINT, STRING, and/or I2D (see all 8)About this table
Gene Ontology (GO): 1 biological process term (GO ID links to tree view): About this table | GO ID | Qualified GO term | Evidence | PubMed IDs |
|---|
| GO:0008053 | mitochondrial fusion |
IMP | -- |
SMCR7L for ontologies About GeneDecksing
|
Drugs & Compounds for SMCR7L gene(Chemical Compounds according to UniProtKB, Enzo Life Sciences,
EMD Millipore, Tocris Bioscience
HMDB,
BitterDB, and/or
Novoseek, and Drugs according to
DrugBank,
Enzo Life Sciences, and/or
PharmGKB, with drugs/clinical trials/news
search links to CenterWatch)
About This Section
|
Browse Tocris compounds for SMCR7L Search CenterWatch for drugs/clinical trials and news about SMCR7L / MID51 
|
Transcripts for SMCR7L gene(Secondary structures according to
fRNAdb,
GenBank/EMBL/DDBJ Accessions according to
Unigene
(Build 235 Homo sapiens; Mar 10 2013) or GenBank, RefSeq according to Entrez Gene,
DOTS (version 10), and/or
AceView,
transcript ids from Ensembl
with links to UCSC,
exon structure from GeneLoc,
alternative splicing isoforms according to ASD and/or
ECgene,
RNAi Products from
EMD Millipore,
siRNAs from
OriGene,
QIAGEN,
shRNA from
OriGene,
Sirion Biotech,
microRNA from QIAGEN,
Tagged/untagged cDNA clones from
OriGene,
SwitchGear Genomics,
GenScript,
DNA2.0,
Vector BioLabs,
Primers from
OriGene,
SABiosciences, and/or
QIAGEN
) About This Section
| REFSEQ mRNAs for SMCR7L gene: NM_019008.4 Unigene Cluster for SMCR7L: Smith-Magenis syndrome chromosome region, candidate 7-like Hs.744044 [show with all ESTs]Unigene Representative Sequence: NM_01900814 Ensembl transcripts including schematic representations, and UCSC links where relevant: ENST00000464629 ENST00000402881(uc003axw.3) ENST00000467866 ENST00000465564 ENST00000489792 ENST00000478342 ENST00000481746 ENST00000433117 ENST00000325301(uc003axx.3 uc003axy.3) ENST00000494219 ENST00000404569(uc010gxz.1) ENST00000434364 ENST00000428069 ENST00000479514
Clone Products: |  | OriGene Myc/DDK tagged cDNA clones in CMV expression vector in human, mouse, rat for SMCR7L (see all 3) OriGene untagged cDNA clones in CMV expression vector in human, mouse, rat for SMCR7L OriGene custom cloning services - gene synthesis, subcloning, mutagenesis,
variant library, vector shuttling 
| |  | GenScript: all cDNA clones in your preferred vector: SMCR7L (NM_019008) | |  | DNA2.0 Custom Codon Optimized Gene
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Additional cDNA sequence: AF086364.1 AK000239.1 AK026539.1 AL136768.1 AL365515.1 BC002587.2 BC002861.2 BC008327.1 BC032530.2 BC047292.1 BC054037.1 15 DOTS entries: DT.453511 DT.100784245 DT.97845999 DT.75154178 DT.95092313 DT.100784244 DT.92455424 DT.95312221 DT.120674539 DT.95312200 DT.100029590 DT.120674544 DT.95253353 DT.95312217 DT.100829998 24/2626 AceView cDNA sequences (see all 2626): BI063069 CR617911 CA414907 CB127079 AA251361 BI064081 BM453092 CB130958 BX418350 AW001098 BM667623 BM848305 CA417306 AW243681 BE205929 CD368567 BU185187 CA445135 BQ001015 CR599519 CR605724 BM716193 BM452714 AA730076 GeneLoc Exon Structure
5/17 Alternative Splicing Database (ASD) splice patterns (SP) for SMCR7L (see all 17) About this scheme
| ExUns: | 1 | ^ | 2 | ^ | 3 | ^ | 4a | · | 4b | · | 4c | · | 4d | · | 4e | · | 4f | ^ | 5 | ^ | 6 | ^ | 7 | ^ | 8a | · | 8b | · | 8c | · | 8d | · | 8e | ^ | 9a | · | 9b | · | 9c | ^ | 10 | ^ | 11a | · | 11b | · | 11c | ^ | 12a | · | 12b | ^ | |
| SP1: | |   | |   | |   | |   | |   | |   | |   | |   | |   | - |   | - |   | - |   | |   | |   | |   | |   | |   | |   | |   | |   | - |   | - |   | - |   | - |   | |   | |   | |
| SP2: | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | - |   | - |   | - |   | - |   | |   | |   | |
| SP3: | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | - |   | - |   | |   | |   | |   | |   | |
| SP4: | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |
| SP5: | |   | |   | |   | - |   | - |   | |   | |   | |   | |   | - |   | - |   | - |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   |
| ExUns: | 13a | · | 13b | · | 13c | ^ | 14a | · | 14b | · | 14c | · | 14d | · | 14e | · | 14f | ^ | 15 | |
| SP1: | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |
| SP2: | |   | |   | |   | - |   | |   | |   | |   | |   | |   | |   | |
| SP3: | |   | |   | |   | - |   | |   | |   | |   | |   | |   | |   | |
| SP4: | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |
| SP5: | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   |
ECgene alternative splicing isoforms for SMCR7L
|
Expression for SMCR7L gene
(RNA expression data according to
H-InvDB,
NONCODE,
miRBase, and
RNAdb,
Expression images according to data from
BioGPS,
Illumina Human BodyMap, and
CGAP
SAGE,
Sets of similar genes according to GeneDecks,
in vivo and in vitro expression data from LifeMap Discovery™,
plus additional links to
Genevestigator, and/or
SOURCE, and/or
BioGPS, and/or
UniProtKB,
PCR Arrays from
SABiosciences,
Primers from
OriGene,
SABiosciences, and/or
QIAGEN,
In Situ Hybridization Assays from Advanced Cell Diagnostics)
About This Section
| SMCR7L expression in normal human tissues (normalized intensities) See probesets specificity/sensitivity at GeneAnnot About this imageBioGPS CGAP TAG: GGAAGAAGAA
 About this image See SMCR7L Protein Expression from SPIRE MOPED and PaxDB Genevestigator expression for SMCR7L
SOURCE GeneReport for Unigene cluster: Hs.744044
UniProtKB/Swiss-Prot: MID51_HUMAN, Q9NQG6Tissue specificity: Expression is relatively high in heart, skeletal muscle, pancreas and kidney SABiosciences Custom PCR Arrays for SMCR7L
Primer Products: |  | OriGene genome-wide validated SYBR primer pairs in human, mouse, rat for SMCR7L Browse OriGene validated miRNA SYBR primer pairs
| |  | SABiosciences RT2 qPCR Primer Assay in human, mouse, rat SMCR7L | |  | QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat SMCR7L | |  | QIAGEN QuantiFast Probe-based Assays in human, mouse, rat SMCR7L | In Situ Assay Products: |
| Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SMCR7L |
Orthologs for SMCR7L gene
(Orthologs according to
1,2HomoloGene (2older version, for species not in 1newer version),
3euGenes,
4SGD
,
5MGI Mar 06 2013,
with possible further links to
Flybase
and/or
WormBase,
and/or
6Ensembl pan taxonomic compara ,
Gene Trees according to Ensembl and
TreeFam)
About This Section
|
This gene was present in the common ancestor of chordates.
Orthologs for SMCR7L gene from 5/12 species (see all 12) About this table
| Organism |
Taxonomic classification |
Gene |
Description |
Human Similarity |
Orthology Type |
Details |
mouse (Mus musculus) |
Mammalia |
Smcr7l1 , 5 |
Smith-Magenis syndrome chromosome region, candidate more1, 5 |
90.78(n)1 97.84(a)1 |
  |
15 (37.85 cM)5 2395551 NM_178719.51 NP_848834.21 802340805 |
chicken (Gallus gallus) |
Aves |
SMCR7L1 |
Smith-Magenis syndrome chromosome region, candidate more |
78.76(n) 86.39(a) |
  |
418012 XM_416248.3 XP_416248.2 |
lizard (Anolis carolinensis) |
Reptilia |
SMCR7L6 |
-- |
86(a) |
1 ↔ 1 |
5(24891473-24894091) |
African clawed frog (Xenopus laevis) |
Amphibia |
Xl.144882 |
Xenopus laevis transcribed sequences |
77.35(n) |
  |
BJ042453.1 |
zebrafish (Danio rerio) |
Actinopterygii |
smcr7a1 |
Smith-Magenis syndrome chromosome region, candidate more |
67.32(n) 71.68(a) |
  |
564985 NM_001083840.1 NP_001077309.1 |
ENSEMBL Gene Tree for SMCR7L (if available) TreeFam Gene Tree for SMCR7L (if available)  |
Paralogs for SMCR7L gene(Paralogs according to
1HomoloGene, 2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68) About This Section
| Paralogs for SMCR7L gene
- SMCR72
3 SIMAP similar genes for SMCR7L using alignment to 4 protein entries: MID51_HUMAN (see all proteins):DKFZp434F0116 DKFZp434E0130 SMCR7
SMCR7L for paralogs About GeneDecksing
|
Genomic Variants for SMCR7L gene(SNPs/Variants according to the
1NCBI SNP Database,
2Ensembl,
3PupaSUITE,
UniProtKB, and
DNA2.0,
Linkage Disequilibrium by HapMap,
Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene
Mutation Database (HGMD) and the Locus Specific Mutation
Databases (LSDB), Blood group antigen gene mutations by BGMUT,
Resequencing Primers from QIAGEN,
Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
About This Section
|
| Genomic Data | Transcription Related Data | Allele Frequencies | | SNP ID | Valid | Clinical significance | Chr 22 pos | Sequence | # | AA Chg | Type | More | # | Allele freq | Pop | Total sample | More |
|---|
HapMap Linkage Disequilibrium report for SMCR7L (39895437 - 39914137 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions) Database of Genomic Variants (DGV) variations for SMCR7L: --  | SABiosciences Cancer Mutation PCR Assays |
|  | QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing SMCR7L |
|
Disorders
/ Diseases for SMCR7L gene
(in which this Gene is Involved, According to MalaCards,
OMIM, UniProtKB,
the University of Copenhagen DISEASES
database,
Genatlas, GeneTests,
GAD,
HuGE Navigator,
and/or TGDB.)
About This Section
|
SMCR7L for disorders About GeneDecksing
3 diseases for SMCR7L: About MalaCardssmith-magenis syndrome aids dementia complex dementia Human Genome Epidemiology (HuGE) Navigator: SMCR7L (1 document) Export disorders for SMCR7L gene to outside databases
|
Publications for SMCR7L gene (in
PubMed.
Associations of this gene to articles via
1Entrez Gene,
2UniProtKB/Swiss-Prot,
3HGNC,
4GAD,
5PharmGKB,
6HMDB,
7DrugBank,
8UniProtKB/TrEMBL,
9 Novoseek, and/or
10fRNAdb)
About This Section
|
PubMed articles for SMCR7L gene, integrated from 9 sources (see all 19): (articles sorted by number of sources associating them with SMCR7L) | |  | Utopia: connect your pdf to the dynamic world of online information |
- Human MIEF1 recruits Drp1 to mitochondrial outer memb ranes and promotes mitochondrial fusion rather than fission. (PubMed id 21701560)1, 2, 3 Zhao J....NistAcr M. (2011)
- MiD49 and MiD51, new components of the mitochondrial fission machinery. (PubMed id 21508961)1, 2, 3 Palmer C.S....Ryan M.T. (2011)
- The DNA sequence of human chromosome 22. (PubMed id 10591208)1, 2 Dunham I....O'Brien K.P. (1999)
- Mass spectrometric analysis of lysine ubiquitylation r eveals promiscuity at site level. (PubMed id 21139048)1 Danielsen J.M....Nielsen M.L. (2011)
- Genetic variants in nuclear-encoded mitochondrial gen es influence AIDS progression. (PubMed id 20877624)1 Hendrickson S.L....O'Brien S.J. (2010)
- Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle. (PubMed id 18691976)2 Daub H.... Mann M. (2008)
- A quantitative atlas of mitotic phosphorylation. (PubMed id 18669648)2 Dephoure N.... Gygi S.P. (2008)
- The LIFEdb database in 2006. (PubMed id 16381901)1 Mehrle A....Wiemann S. (2006)
- Towards a proteome-scale map of the human protein-protein interaction network. (PubMed id 16189514)1 Rual J.F....Vidal M. (2005)
- Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization. (PubMed id 15324660)1 Jin J....Pawson T. (2004)
|
External Searches for SMCR7L gene
(in PubMed,
OMIM, and NCBI Bookshelf) About This Section
|
|
Genome Databases showing SMCR7L gene
(According to
Entrez Gene,
HGNC,
AceView,
euGenes,
Ensembl,
miRBase,
ECgene,
Kegg,
and/or
H-InvDB)
About This Section
|
|
Other Databases showing SMCR7L gene
(According to HUGE)
About This Section
| -- |
Specialized Databases showing SMCR7L gene(According to PharmGKB,
ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL, Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot) About This Section
|
| Name | Description |
| PharmGKB entry for SMCR7L | Pharmacogenomics, SNPs, Pathways |
|
| | |
About This Section
| Patent Information for SMCR7L gene: Search GeneIP for patents involving SMCR7L
GeneCards and IP: Japan Patent Office Licenses GeneCards European Patent Office Licenses GeneCards Improving the IP Search
|
Products for SMCR7L gene(Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0 and Sirion Biotech, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript, LifeMap BioReagents, and Sirion Biotech, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or
Enzo Life Sciences, In Situ Hybridization Assays from Advanced Cell Diagnostics, Animal models from inGenious Targeting Laboratory) About This Section
|
 | |
 | |
 |
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| | | | Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SMCR7L |
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