MACROH2A1 (NM_004893) Human Untagged Clone

CAT#: SC110068

H2AFY (untagged)-Human H2A histone family, member Y (H2AFY), transcript variant 2


  "NM_004893" in other vectors (4)

Reconstitution Protocol

USD 457.00

In Stock*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol MACROH2A1
Synonyms H2A.y; H2A/y; H2AF12M; H2AFY; MACROH2A1.1; macroH2A1.2; mH2A1
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>NCBI ORF sequence for NM_004893, the custom clone sequence may differ by one or more nucleotides


ATGTCGAGCCGCGGTGGGAAGAAGAAGTCCACCAAGACGTCCAGGTCTGCCAAAGCAGGAGTCATCTTTC
CCGTGGGGCGGATGCTGCGGTACATCAAGAAAGGCCACCCCAAGTACAGGATTGGAGTGGGGGCACCCGT
GTACATGGCCGCCGTCCTGGAATACCTGACAGCGGAGATTCTGGAGCTGGCTGGCAATGCAGCGAGAGAC
AACAAGAAGGGACGGGTCACACCCCGGCACATCCTGCTGGCTGTGGCCAATGATGAAGAGCTGAATCAGC
TGCTAAAAGGAGTCACCATAGCCAGTGGGGGTGTGTTACCCAACATCCACCCCGAGTTGCTAGCGAAGAA
GCGGGGATCCAAAGGAAAGTTGGAAGCCATCATCACACCACCCCCAGCCAAAAAGGCCAAGTCTCCATCC
CAGAAGAAGCCTGTATCTAAAAAAGCAGGAGGCAAGAAAGGGGCCCGGAAATCCAAGAAGCAGGGTGAAG
TCAGTAAGGCAGCCAGCGCCGACAGCACAACCGAGGGCACACCTGCCGACGGCTTCACAGTCCTCTCCAC
CAAGAGCCTCTTCCTTGGCCAGAAGCTGAACCTTATTCACAGTGAAATCAGTAATTTAGCCGGCTTTGAG
GTGGAGGCCATAATCAATCCTACCAATGCTGACATTGACCTTAAAGATGACCTAGGAAACACGCTGGAGA
AGAAAGGTGGCAAGGAGTTTGTGGAAGCTGTCCTGGAACTCCGGAAAAAGAACGGGCCCTTGGAAGTAGC
TGGAGCTGCTGTCAGCGCAGGCCATGGCCTGCCTGCCAAGTTTGTGATCCACTGTAATAGTCCAGTTTGG
GGTGCAGACAAGTGTGAAGAACTTCTGGAAAAGACAGTGAAAAACTGCTTGGCCCTGGCTGATGATAAGA
AGCTGAAATCCATTGCATTTCCATCCATCGGCAGCGGCAGGAACGGTTTTCCAAAGCAGACAGCAGCTCA
GCTGATTCTGAAGGCCATCTCCAGTTACTTCGTGTCTACAATGTCCTCTTCCATCAAAACGGTGTACTTC
GTGCTTTTTGACAGCGAGAGTATAGGCATCTATGTGCAGGAAATGGCCAAGCTGGACGCCAACTAG


>OriGene 5' read for NM_004893 unedited
CATTTTGTAATACGACTCACTTATAGGGCGGCCGCGATTCGACTCGAGGGTCAAGGCCGG
GGCGCCGGGCGGCACGGGCGCGGAGGCCGGACGCTCGGGGCCGCGAAGGGATGTGACGAG
CGGCGCGCTGTGCATTGTGGGAAGCCGGCCGCGAGGACTGGTTCCAGTTCACTCGGCAGC
GGCGCCGGGCGGAGGGGGAGAGCGCGGGCCGCGCGGGCGGGAAGCGAAGAGGCGGGCGGG
CCAGCGAGGAGCGCGGAGAGAAAAGGCGCGAGCGGCCAGGAGGGCTCAGGCCGAGACACC
TTGCAGCTGCCGCCGCCGCCACCGAGCCGCCGCTGTGCTCACTGATCCGCCTCCAGGGCC
ACCGCCATGTCGAGCCGCGGTGGGAAGAAGAAGTCCACCAAGACGTCCAGGTCTGCCAAA
GCAGGAGTCATCTTTCCCGTGGGGCGGATGCTGCGGTACATCAAGAAAGGCCACCCCAAG
TACAGGATTGGAGTGGGGGCACCCGTGTACATGGCCGCCGTCCTGGAGTACCTGACAGCG
GAGATTCTGGAGCTGGCTGGCAATGCAGCGAGAGACAACAAGAAGGGACGGGTCACACCC
CGGCACATCCTGCTGGCTGTGGCCAATGATGAAGAGCTGAATCAGCTGCTAAAAGGAGTC
ACCATAGCCAGTGGGGGTGTGTTACCCCACATCCACCCCGAGTTGCTAGCGAACAAGCGG
GGATCCAAAGGAAAGTTGGAAGCCATCATCACACCACCCCCCAGCCCAAAAGGCCAAGTT
CTCCAATCCCAGAGTAAGCCTGTTTCCTAAAAAGCATGAAGCACAGAAGGGTGCCCCGGA
AATCCAAGAAACCAGGTTGAGTCCATTAAGGCAGCCAGTGCCGACAGCACAACCGAGGGC
CACCTGCCGAAGGCTTCCAGTTCTTTTCCCCAATAGCCTCTTCTTGGCCACAATTGCAGT
TGTCAAGCTGACTTTGCTCCATCGCACGGATC
>OriGene 3' read for NM_004893 unedited
NGCCTTACTTGNCCGCGCCCGCTATCTANGATCGGTTTTTCTTTTTTTTTTTTTTTTTTT
TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAACGGGTAAACATTTTACTA
AATCAACTCACACAAATTCCAAATTGCAAATTTAATTAAGGACAACAGATTCTGGTTTGC
CTTATTAAATCTTTCATTTTCAAACCCCTCAATAAAACAAAAAGCACCCCAAAATTAGGT
CTGGGGCAAATTCATGATTCTTTTGGGGGGGGAACCCAAAAAAACCTTAAAGTAAAAAAA
ACCCCCCTGGGGGATGTCCAATAAAGCCCCACAACACCCGCTTACAAACGGGGCTCCCTG
GCTTCGGGGACAGGAAAAAAACCCTGTCCTCCCCACTGGTGGGCGGCAATCAGGGTTTCC
TTAAAACAAAACTATAAAACCCCCTAGGTTACACTAAGTCAAACCCCGTCTGGAACACAG
GGTTTAACAACAGAAATGCCCACTATAAGGGTCAACATAAAAACTTTTTAAAAGGGCAAA
AACAATTAAACCGGAACCCCAAGCCTTATTTTCCCTAAATGACCAAACCTGAAAAAGAAA
GGGGCCCCCCCTCCCACTAGGAGGGAAGGGGCTTTTTTTTTTTTTTTAAACTGAAGGGGG
GGCCACTGGGGCACCCGTTTTTGTCCTTTCTCACACTAATTGGGCCCCACCTTGGCCCTT
TCCTGCCAAAAAACGCCTATACTCCCTGTGCCAAAAGCACCAAACCCCCCCTTTGGTGGA
AAAGCCCTTGGAACCCCAAAAACTGGAAGGCCCCTCAAAAACCCTGACTTTCCGTCGTCT
TGAAAACCCCTTCCCCCCCCCCCCAGGGGGGAACACCACGGACCC
Restriction Sites NotI-NotI     
ACCN NM_004893
Insert Size 2100 bp
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
Reconstitution 1. Centrifuge at 5,000xg for 5min.
2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
Reference Data
RefSeq NM_004893.2, NP_004884.1
RefSeq Size 1923 bp
RefSeq ORF 1116 bp
Locus ID 9555
UniProt ID O75367
Cytogenetics 5q31.1
Domains H2A, A1pp, histone
Protein Pathways Systemic lupus erythematosus
Gene Summary Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-independent histone that is a member of the histone H2A family. It replaces conventional H2A histones in a subset of nucleosomes where it represses transcription and participates in stable X chromosome inactivation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2015]
Transcript Variant: This variant (2) has a unique 5' UTR and uses an alternate splice site in its coding region, compared to variant 3. This results in a protein (isoform 2) that is a single amino acid shorter than isoform 3. Variants 2 and 4 encode the same isoform (2). Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments.

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