ABS2121

Anti-ALAS-E

from rabbit

Manufacturer: Sigma Aldrich

Synonym(S): Erythroid-specific 5-aminolevulinate synthase mitochondrial, EC: 2.3.1.37, ALAS-E, 5-aminolevulinic acid synthase 2, Delta-ALA synthase 2, Delta-aminolevulinate synthase 2

Select a Size

Pack Size SKU Availability Price
100 μL ABS2121-100-μL In Stock ₹ 36,880.00

ABS2121 - 100 μL

₹ 36,880.00

In Stock

Quantity

1

Base Price: ₹ 36,880.00

GST (18%): ₹ 6,638.40

Total Price: ₹ 43,518.40

biological source

rabbit

Quality Level

100

antibody form

unpurified

antibody product type

primary antibodies

clone

polyclonal

species reactivity

human

packaging

antibody small pack of 25 μL

technique(s)

western blot: suitable

isotype

IgG

NCBI accession no.

NP_000023

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Description

  • General description: 5-aminolevulinate synthase, erythroid-specific, mitochondrial (UniProt: P22557; also known as EC: 2.3.1.37, ALAS-E, 5-aminolevulinic acid synthase 2, ALAS2, Delta-ALA synthase 2, Delta-aminolevulinate synthase 2) is encoded by the ALAS2 (also known as ALASE, ASB) gene (Gene ID: 212) in human. Two forms of ALAS have been described in literature; ALAS1 (ALAS-H) and ALAS2 (ALAS-E). ALAS-H is a housekeeping protein, which mediates synthesis of early heme in the mitochondria of most cells. ALAS-E is a mitochondrial matrix homodimeric enzyme that is also involved in catalyzing the first step in heme biosynthetic pathway. Four isoforms of ALAS-E have been described that are generated by alternate splicing. ALAS-E is synthesized with a transit peptide (aa 1-49) that is cleaved to generate a mature form (aa 50-587). Defects in ALAS2 gene are linked to sideroblastic anemia that is characterized by anemia, hypochromic peripheral erythrocytes, systemic iron overload, and by the presence of bone marrow ringed sideroblasts. Defects in ALAS2 gene are also reported in X-linked dominant form of erythropoietic protoporphyria that is characterized by accumulation and increased excretion of porphyrins or their precursors.
  • Specificity: This rabbit polyclonal antibody detects erythroid-specifc 5-aminolevulinate synthase, mitochondrial in human cells.
  • Immunogen: Epitope: unknown
  • Application: Anti-ALAS-E, Cat. No. ABS2121, is a rabbit polyclonal antibody that detects 5-aminolevulinate synthase, erythroid-specific, mitochondrial and has been tested for use in Western Blotting.
  • Quality: Evaluated by Western Blotting with recombinant hALAS2Western Blotting Analysis: A 1:2,000 dilution of this antibody detected recombinant ALAS-E.
  • Target description: ~58 and 72 kDa observed; Detects both the precusor and mature forms of human ALAS2. Uncharacterized bands may be observed in some lysate(s).
  • Physical form: Format: Unpurified
  • Storage and Stability: Stable for 1 year at -20°C from date of receipt.Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
  • Other Notes: Concentration: Please refer to lot specific datasheet.
  • Disclaimer: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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biological source:
rabbit

Quality Level:
100

antibody form:
unpurified

antibody product type:
primary antibodies

clone:
polyclonal

species reactivity:
human

packaging:
antibody small pack of 25 μL

technique(s):
western blot: suitable

isotype:
IgG

NCBI accession no.:
NP_000023

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