ALAS1 Recombinant Monoclonal Antibody

Code CSB-RA266893A0HU
Size US$210
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  • Western Blot
    Positive WB detected in: Hela whole cell lysate, HepG2 whole cell lysate, Raji whole cell lysate, PC-3 whole cell lysate, A549 whole cell lysate, MCF-7 whole cell lysate
    All lanes: ALAS1 antibody at 1:1500
    Secondary
    Goat polyclonal to rabbit IgG at 1/50000 dilution
    Predicted band size: 71, 13 kDa
    Observed band size: 71 kDa
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Product Details

Uniprot No.
Target Names
ALAS1
Alternative Names
5-aminolevulinate synthase, nonspecific, mitochondrial (ALAS-H) (EC 2.3.1.37) (5-aminolevulinic acid synthase 1) (Delta-ALA synthase 1) (Delta-aminolevulinate synthase 1), ALAS1, ALAS3 ALASH
Species Reactivity
Human
Immunogen
A synthesized peptide derived from human Alas1
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Monoclonal
Isotype
Rabbit IgG
Clone No.
2A9
Purification Method
Affinity-chromatography
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Rabbit IgG in 10mM phosphate buffered saline , pH 7.4, 150mM sodium chloride, 0.05% BSA, 0.02% sodium azide and 50% glycerol.
Form
Liquid
Tested Applications
ELISA, WB
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:5000
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Description

ALAS1 (5-aminolevulinate synthase 1) serves as the rate-limiting enzyme in the heme biosynthesis pathway, catalyzing the first and most critical step of porphyrin production in the mitochondria. This housekeeping enzyme plays a fundamental role in maintaining cellular heme homeostasis across virtually all tissues, making it a key target for researchers investigating metabolic disorders, cardiovascular biology, and the signaling pathways that regulate cellular energy metabolism.

This recombinant monoclonal antibody, clone 2A9, offers the reproducibility and consistency that demanding experimental workflows require. Because the antibody sequence is defined and produced recombinantly in rabbit host cells, researchers can expect reliable performance across experiments and over time, eliminating the lot-to-lot variability that can complicate long-term studies or multi-site collaborations.

Validation by western blot demonstrates robust detection of ALAS1 at the expected 71 kDa molecular weight across a diverse panel of human cell lines, including HeLa, HepG2, Raji, PC-3, A549, and MCF-7. This broad validation across epithelial, hepatic, lymphoid, and carcinoma-derived cells confirms the antibody's utility for studying ALAS1 expression in multiple experimental contexts. The recommended working dilution range of 1:500 to 1:5000 for western blot applications provides flexibility to optimize signal intensity based on your specific sample type and detection system.

Supplied in a glycerol-containing buffer optimized for long-term storage stability, this affinity-purified antibody is well-suited for researchers exploring heme metabolism, mitochondrial function, and the regulatory networks connecting cellular metabolism to cardiovascular physiology and signal transduction pathways.

Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Gene References into Functions
  1. The mutation in CLPX inactivates its ATPase activity, resulting in coassembly of mutant and WT protomers to form an enzyme with reduced activity. The presence of low-activity CLPX increases the posttranslational stability of ALAS, causing increased ALAS protein and ALA levels, leading to abnormal accumulation of PPIX. PMID: 28874591
  2. the heme-binding site in the N-terminal region of the mature ALAS1 protein is also necessary for the heme-dependent oxidation of ALAS1. PMID: 27496948
  3. ALAS1 mRNA and activity were elevated approximately ~3- and 5-fold, and HMB synthase activity was approximately half-normal (~42%) PMID: 26062020
  4. The -853T variant functions as an enhancer in the presence of estrogen and speculates that the -1253A variant reduces transcription activity. PMID: 19656447
  5. These results indicate that ALAS1 is a novel NR5A-target gene and participates in steroid hormone production. PMID: 23024262
  6. Lon peptidase 1 (LONP1)-dependent breakdown of mitochondrial 5-aminolevulinic acid synthase protein by heme in human liver cells. PMID: 21659532
  7. REVIEW:active site and mechanistic analysis, protein folding, structure and function. PMID: 11929042
  8. REVIEW: mechanisms involving ALAS deficiency, point mutations, post translational processing, and complex formation with succinyl CoA synthetase subunit B in the pathogenesis of hereditary sideroblastic anemia. PMID: 11929048
  9. ALAS expression is regulated by AP-1 complex through sequestration of cAMP-response element protein (CRE)-binding protein (CBP) coactivator in human cells PMID: 12433930
  10. ALAS gene expression is regulated by Hepatic nuclear factor 3 and nuclear factor 1 PMID: 15123725
  11. First described frameshift ALAS2 mutation, CD506-507 (-C). PMID: 15477213
  12. in the liver of Acute liver failure patients, there may be an increase in free heme concentration which down-regulating ALAS1 gene expression PMID: 15547665
  13. Alternative splicing of human ALAS1 generates two mRNAs with different 5'-UTRs: a major one, where exon 1B is omitted, and a minor form containing exon 1B. PMID: 15710391
  14. 5-aminolevulinate synthase gene repression by the potent tumor promoter, TPA, involves multiple signal transduction pathways PMID: 15797241
  15. Expression of candidate genes HPRT1 and ALAS1 in malignant and non-malignant prostate tissue samples after microdissection. PMID: 17628775
  16. Differential regulation of human ALAS1 mRNA and protein levels by heme and cobalt protoporphyrin. PMID: 18719978
  17. In this study, we show significant reductions of the rate-limiting enzymes involved in heme biosynthesis, ALAS1 in the postmortem cortex of Alzheimer's disease subjects, providing additional evidence of abnormal heme homeostasis in Alzheimer's disease. PMID: 19477221

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Subcellular Location
Mitochondrion matrix.
Protein Families
Class-II pyridoxal-phosphate-dependent aminotransferase family
Database Links

HGNC: 396

OMIM: 125290

KEGG: hsa:211

STRING: 9606.ENSP00000309259

UniGene: Hs.476308

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