HAX1 (NM_006118) Human Untagged Clone

CAT#: SC116339

HAX1 (untagged)-Human HCLS1 associated protein X-1 (HAX1), transcript variant 1


  "NM_006118" in other vectors (6)

Reconstitution Protocol

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol HAX1
Synonyms HCLSBP1; HS1BP1; SCN3
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC116339 sequence for NM_006118 edited (data generated by NextGen Sequencing)
ATGAGCCTCTTTGATCTCTTCCGGGGCTTTTTCGGCTTTCCTGGACCTCGGAGCCACAGA
GATCCCTTTTTTGGAGGGATGACTCGAGATGAAGATGATGATGAGGAAGAAGAAGAAGAA
GGGGGCTCATGGGGCCGTGGGAACCCAAGGTTCCATAGTCCTCAGCACCCCCCTGAGGAA
TTTGGCTTCGGCTTCAGCTTCAGCCCAGGAGGAGGGATACGTTTCCACGATAACTTCGGC
TTTGATGACCTAGTACGAGATTTCAATAGCATCTTCAGCGATATGGGGGCCTGGACCTTG
CCTTCCCATCCTCCTGAACTTCCAGGTCCTGAGTCAGAGACACCTGGTGAGAGACTACGG
GAGGGACAGACACTTCGGGACTCAATGCTTAAGTATCCAGATAGTCACCAGCCCAGGATC
TTTGGGGGGGTCTTGGAGAGTGATGCAAGAAGTGAATCCCCCCAACCAGCACCAGACTGG
GGCTCCCAGAGGCCATTTCATAGGTTTGATGATGTATGGCCTATGGACCCCCATCCTAGA
ACCAGAGAGGACAATGATCTTGATTCCCAGGTTTCCCAGGAGGGTCTTGGCCCGGTTCTA
CAGCCCCAGCCCAAATCCTATTTCAAGAGCATCTCTGTGACCAAGATCACTAAACCAGAT
GGGATAGTGGAGGAGCGCCGGACTGTGGTGGACAGTGAGGGCCGGACAGAGACTACAGTA
ACCCGACACGAAGCAGATAGCAGTCCTAGGGGTGATCCAGAATCACCAAGACCTCCAGCC
CTGGATGATGCCTTTTCCATCCTGGACTTATTCCTGGGACGTTGGTTCCGGTCCCGGTAG

Clone variation with respect to NM_006118.3
>OriGene 5' read for NM_006118 unedited
ATTTTGTAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACGAGGAATTTCTCACAG
GGCTGCGCAGGTTTCCCCCGTCTGCGAATGGACCACTGGAGGGGTTCAAAGGTTCGCGTC
CCAGTACGGGAATGAGCCTCTTTGATCTCTTCCGGGGCTTTTTCGGCTTTCCTGGACCTC
GGAGCCACAGAGATCCCTTTTTTGGAGGGATGACTCGAGATGAAGATGATGATGAGGAAG
AAGAAGAAGAAGGGGGCTCATGGGGCCGTGGGAACCCAAGGTTCCATAGTCCTCAGCACC
CCCCTGAGGAATTTGGCTTCGGCTTCAGCTTCAGCCCAGGAGGAGGGATACGTTTCCACG
ATAACTTCGGCTTTGATGACCTAGTACGAGATTTCAATAGCATCTTCAGCGATATGGGGG
CCTGGACCTTGCCTTCCCATCCTCCTGAACTTCCAGGTCCTGAGTCAGAGACACCTGGTG
AGAGACTACGGGAGGGACAGACACTTCGGGACTCAATGCTTAAGTATCCAGATAGTCACC
AGCCCAGGATCTTTGGGGGGGTCTTGGAGAGTGATGCAAGAAGTGAATCCCCCCAACCAG
CACCAGACTGGGGCTCCCAGAGGCCATTTCATAGGTTTGATGATGTATGGCCTATGGACC
CCCATCCTAGAACCAGAGAGGACANTGATCTTGATTCCCAGGTTTTCCAGGAGGGTCTTG
GCCCGGTTCTACAGCCCCAGCCCAAATCCTATTTCAAGAGCATCTCTGTGACCAAGATCA
CTAAACCAGATGGGATAGTGGAGGAGCGCCGGACTGTGGTTNACAGTTGAGGCCGGACAA
GACTCAGTAACCCGACACGAGCAGATAC
>OriGene 3' read for NM_006118 unedited
GGCCGCAATTTANAGTCGAGNTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTAAATA
AAGGTTTTATTGGTCAGTTTGGGTGAGTGACAAACTGACATGGCCCCAGTTCACTATTCC
ACATATCCAAGCCCCTGAGGTGGCAAGAGAAGCTAAGCTTATTAATGGTGGGCAATGGGT
GAAAGGTGGAAAGGACTTGAAGGCCTCTGAGGGTTAACAAGGCTACCGGGACCGGAACCA
ACGTCCCAGGAATAAGTCCAGGATGGAAAAGGCATCATCCAGGGCTGGAGGTCTTGGTGA
TTCTGGATCACCCCTAGGACTGCTATCTGCTTCGTGTCGGGTTACTGTAGTCTCTGTCCG
GCCCTCACTGTCCACCACAGTCCGGCGCTCCTCCACTATCCCATCTGGTTTAGTGATCTT
GGTCACAGAGATGCTCTTGAAATAGGATTTGGGCTGGGGCTGTACAACCGGGCCAAGACC
CTCCTGGGAAACCTGGGAATCAAGATCATTGTCCTCTCTGCGTCTAGGATGGGGGTCCAT
AGGCCATACCTTATCAAACCTATGAAATGGCCTCTGGGACCCCACTCTGGCGCTGGTTGG
GGGGATTCACCTTTTGCATCACTCTCCAAGACCCCCCAAAAATCCTGGGGCTGCGACTAT
TTGGATACTTAAACCCTTGGGTCCCCAAGCGGCTGCCCCTTCCCCGATCCCCTCACCAGG
TGCCCCTGCCTCAGCCCTCCACATCTCCGAGGATGGGAAGGCAAGGTCCAGCCCCCATCT
TCTCAACATCCTTCTGAAACCTCCTCCATGTCCATCACCGCCCCAGCCTTCGGGGAAACC
GTCCCCTTTCTCCGGGCGTTAAACTTGACCCTAACCCTCATCCTCCACGGCGGGGCCGCA
GATTCGTTCATCTTCGGTCCCACTGGACACTTAGACCCCCCCTTTTTTTTCTCCCTCCAC
CCTTTTNTTGTCCGCGNTCCCCCCAGACGGCACTCTTGGGT
Restriction Sites NotI-NotI     
ACCN NM_006118
ORF Size 840 bp
Insert Size 1090
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).
Reference Data
RefSeq NM_006118.3, NP_006109.2
RefSeq Size 1196
RefSeq ORF 840
Locus ID 10456
Gene Summary The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin. It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body. Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (a).

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