LETM1 antibody (AA 1-140)

Catalog No. ABIN7268225

Product Details anti-LETM1 Antibody

Target: LETM1 (Leucine Zipper-EF-Hand Containing Transmembrane Protein 1 (LETM1))

Binding Specificity: AA 1-140

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This LETM1 antibody is un-conjugated

Application: Western Blotting (WB)

Purpose: LETM1 Rabbit pAb

Sequence: MASILLRSCR GRAPARLPPP PRYTVPRGSP GDPAHLSCAS TLGLRNCLNV PFGCCTPIHP VYTSSRGDHL GCWALRPECL RIVSRAPWTS TSVGFVAVGP QCLPVRGWHS SRPVRDDSVV EKSLKSLKDK NKKLEEGGPV

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-140 of human LETM1 (NP_036450.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for LETM1

Target: LETM1 (Leucine Zipper-EF-Hand Containing Transmembrane Protein 1 (LETM1))

Alternative Name: LETM1 (LETM1 Products)

Synonyms: LETM1 antibody, wu:fc31h08 antibody, wu:fc58h01 antibody, zgc:109969 antibody, letm1 antibody, MGC145623 antibody, leucine zipper and EF-hand containing transmembrane protein 1 antibody, leucine zipper-EF-hand containing transmembrane protein 1 antibody, LETM1 and EF-hand domain-containing protein 1, mitochondrial antibody, LETM1 antibody, letm1 antibody, LOC100346816 antibody, Letm1 antibody

Background: This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.,LETM1,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial Biogenesis,Mitochondrial markers,LETM1

Molecular Weight: 29kDa/33kDa/83kDa

Gene ID: 3954

UniProt: O95202